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Current Organic Synthesis, 2019, 16, 615-649

615

REVIEW ARTICLE

Organic Synthesis Using Environmentally Benign Acid Catalysis

Anne Kokel1, Christian Schäfer1,* and Béla Török1,*

1Department of Chemistry, University of Massachusetts Boston, 100 Morissey Blvd., Boston, MA 02125, USA

A R T I C L E H I S T O R Y

Received: October 09, 2018 Revised: November 28, 2018 Accepted: January 11, 2019 DOI: 10.2174/1570179416666190206141028

Abstract: Recent advances in the application of environmentally benign acid catalysts in

organic synthesis are reviewed. The work includes three main parts; (i) description of

environmentally benign acid catalysts, (ii) synthesis with heterogeneous and (iii)

homogeneous catalysts. The first part provides a brief overview of acid catalysts, both solid acids (metal oxides, zeolites, clays, ion-exchange resins, metal-organic framework

based catalysts) and those that are soluble in green solvents (water, alcohols) and at the

same time could be regenerated after reactions (metal triflates, heteropoly acids, acidic

organocatalysts etc.). The synthesis sections review a broad array of the most common

and practical reactions such as Friedel-Crafts and related reactions (acylation, alkylations,

hydroxyalkylations, halogenations, nitrations etc.), multicomponent reactions, rearrange-ments and ring transformations (cyclizations, ring opening). Both the heterogeneous and homogeneous

catalytic synthesis parts include an overview of asymmetric acid catalysis with chiral Lewis and Brønsted

acids. Although a broad array of catalytic processes are discussed, emphasis is placed on applications with

commercially available catalysts as well as those of sustainable nature; thus individual examples are critically

reviewed regarding their contribution to sustainable synthesis.

Keywords: Solid acid, heterogeneous catalysis, metal oxides, clay, zeolite, metal-organic-frameworks, heteropoly acids, ion-exchange resins, sulfated metal oxides.

1. INTRODUCTION

Acidity-basicity is one of the oldest concepts in the history of chemistry beginning with Lavoisier and Davy over two centuries ago [1]. While the first general description was developed by Arrhenius [2], it was later refined and replaced by the Brønsted-Lowry [3] and Lewis [4] concepts. Accordingly, acid catalysis has extensive history that covers a broad range of applications such as electrophilic addition, esterification, ester hydrolysis, aromatic electrophilic substitution or rearrangement reactions [5]. Con-ventional mineral acids, such as HCl, H2SO4 or HNO3 were the traditional catalysts of choice for these transformations. Despite their usefulness, these acids are highly corrosive; many of them release gases that pose safety and health hazards. In addition, most of them are impossible to reuse. In short, their application is undesirable under the Green Chemistry principles [6]. Due to the importance of acid catalysis, significant efforts were made to address this problem. The two major ways to replace these harmful acids are the application of solid acids via heterogeneous catalytic reactions and the use of homogeneous (soluble) acid catalysts that do not undergo hydrolysis under aqueous conditions and can be recycled. The latter acids are soluble in water and several organic solvents thus acting as homogeneous catalysts. Both groups of catalysts are now frequently used in a broad variety of organic reactions, and are extensively reviewed [7].

In this account we will survey the applications of these catalysts in environmentally benign processes. Although we provide major sources of earlier reviews and books, the emphasis will be placed

*Address correspondence to these authors at the Department of Chemistry, University of Massachusetts Boston, 100 Morissey Blvd., Boston, MA 02125, USA; Tel: +1-617-287-6159; Fax: +1-617-287-6030; E-mails: [email protected] and [email protected]

on recent advances, thus most of the original work reviewed in this article will cover the past decade between 2008 and 2018. Even with this limitation, due to the large number of papers published in this period and the page limitations of this work, the focus will be on providing a broad scope of reactions with representative examples.

2. ENVIRONMENTALLY BENIGN ACID CATALYSTS

Environmentally benign acid catalysts form two major groups depending on the type of catalysis they perform. Solid acids are not soluble in water or organic solvents and the reactions occur on the surface of these materials thus forming heterogeneous catalytic systems. In contrast, there are acids that, although solid under normal conditions, readily dissolve in water and many organic solvents thus performing homogeneous catalysis. In this part we summarize the most frequently used catalyst in both groups (Fig. 1).

It is worth noting that there is a limited overlap between the two major groups. There are several acids, mainly inorganic acids and salts, such as heteropoly acids or metal triflates that are not soluble in certain organic solvents, thus with the appropriate selection of the solvent they can be used as either heterogeneous or homo-geneous catalysts. Their water solubility and stability under aqueous conditions still aid their recycling during work up pro-cedures.

2.1. Heterogeneous Catalysis - Solid Acids

Solid acid catalysts have been extensively used in organic synthesis as well as in the pharmaceutical industry [8]. Their advantages include their practical utility (durability, easy work-up by filtration), their potential recyclability, their low cost and overall their great green potential. These catalysts are of many types

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616 Current Organic Synthesis, 2019, Vol. 16, No. 4 Kokel et al.

depending on the composition and the structure they possess. The aforementioned assets combined with various other specific properties attracted vast interest toward their applications. Due to the polar nature of these materials, most are excellent microwave absorbers thus can act as a catalyst as well as an internal heating medium for a broad array of transformations [9-11]. The main types of solid acid-catalysts; namely metal oxides, zeolites, clays, acidic ion exchange resins, heteropoly acid salts and metal organic frameworks and sulfated metal oxides; will be briefly described in this section.

The first large group of solid acids is based on metal oxides [12]. Although their acidity is relatively limited, due to their broad availability and low cost they represent a versatile group of weak acid catalysts for many transformations [13]. They include the common silica or acidic alumina catalysts. When metal oxides are treated with sulfuric acid they form a special group of catalysts named sulfated metal oxides [14]. The reaction with sulfuric acid appears to enhance the Lewis acid character and significantly strengthen acidity. Some of these materials, such as sulfated zirconia are commonly used Lewis acid catalysts in organic synthesis [15].

Probably the most utilized solid acid catalysts originate from natural aluminosilicates, zeolites and clays, although the success of the natural materials inspired extensive efforts in the preparation of semi-synthetic and synthetic alternatives.

Clays are aluminosilicates constituted of multiple layers of polyhedrons. Tetrahedral silicone oxides and octahedral hydrous alumina are their common building blocks [16]. Clays have demonstrated remarkable catalytic activity due to their porous structure that provides a unique environment in which molecules can interact in specific ways allowing reactions to take place. In other words, they act as a micro-reactor capable of initiating reactions on account of their inherent properties such as adsorption-, swelling- and ion-exchange capacities. Various types of clays exist; depending on their properties, they are suitable for catalyzing a broad scope of transformations [17]. Clays can be classified into two categories: the negatively charged clays that welcome balancing cations and the positively charged clays containing anions in their interlayer space [18]. The second class of clays is often synthesized while the first one is prepared from natural sources, most commonly montmorillonites. The natural clays can be used directly in their original form or after undergoing chemical treatments that enhance an existing characteristic or specifically introduce an extrinsic feature. An acidic activation method is often employed to enhance their acidic properties. To do so, several mineral acid solutions can be applied including phosphoric acid, sulfuric acid or nitric acid [19]. The resulting materials exhibit an increase in acidity and the number of active sites and surface area. The widespread montmorillonites are cationic clays, member of the

smectite group [20], possess remarkable absorption capacity, high surface area as well as interesting acidic properties which altogether contribute to their success as catalysts in various reactions [21]. Montmorillonites K-10 and KSF, both acid treated montmoril-lonites, are the most widely used acidic clays in organic synthesis [22].

Zeolites are also aluminosilicates, however, in contrast to the layered structure of clays these highly porous, crystalline materials exhibiting a well-defined channel and cage-based structure [23] and less commonly a lamellar structure [24]. The molecular dimensions of their channels and cages contribute greatly to the catalytic potential of zeolitic materials [25]. Similarly to clays, the catalytic properties of zeolites are due in part to the exchangeable ions and water molecules trapped in their structure as well as their com-monly high adsorption capacity [26]. It is important to mention that zeolites also offer the possibility to introduce specific active sites and to modulate the existing electronic features giving rise, for example, to zeolites with enhanced acidic properties. In catalysis, the most commonly used acidic zeolites are zeolites X and Y, employed in catalytic cracking, and zeolite ZSM-5, a fundamental catalysts in the petroleum industry [27]. In general, although zeolites are strong acids at high temperatures, their acidity is relatively modest at the common temperature range of organic synthesis [27]. Efforts to prepare zeolites with stronger acid sites by functionalizing them with organic moieties led to promising results; nonetheless, this issue still remains a challenge [26].

Acidic ion exchange resins are versatile materials used as catalysts for many organic transformations as well [28]. Their framework makes possible the synthesis of hybrid materials with tunable acidity. Depending upon their pore size, chemical structure and formulation, they are useful in a number of transformations. Ionic exchange resins exist as either cationic or anionic forms. The so-called acidic ionic exchange resins are typically of cationic type. Amberlyst and Nafion are two common sulfonic acid based-resins employed in numerous catalytic processes [29]. While the Amberlyst type is based on a polystyrene-sulfonic acid motif, Nafion possesses a perfluorinated backbone with sulfonic acid entities.

The high electron withdrawing character of fluorine in Nafion significantly enhances its acidity to the superacidic level. Amberlyts are able to catalyze the conversion of acetals and carbonyls to alcohols, the conversion of acids to esters, among others. Nafion has been successfully employed as solid-acid catalyst for several reaction types such as oxidation reactions, protection and deprotection of alcohols and carbonyl containing compounds, as well as rearrangements [30]. It is worth mentioning that their BET surface area, however, is rather low (~9 m2/g) and they often suffer from a poor porosity. To address these issues and fully take advantage of the strong acidity of Nafion-H a Nafion-silica

Acid Catalysis

Heterogeneous Catalysis Homogeneous Catalysis

metaloxides(SiO2,

Al2O3,TiO2, ZnO etc.)

zeolites(HY, H-ZSM5, etc.)

clays(K-10, KSF etc.)

acidic ion-exchangeresins(Nafion-H, Amberlyst, Dowex, etc.)

heteropolyacids

triflic acid,metal triflates

acidic organo-catalysts

(H4[SiMo12O40],H3[PW12O40]etc.)

(CF3SO3H - TfOH,Ga(OTf)3, Sc(OTf)3 etc.)

amino acids,amine-hydro-chlorideschiral phosphoricacids etc.)

other (heteropolyacid salts,certain triflates,sulfated metaloxides,metal-organicframeworks etc.)

Fig. (1). Classification of green acid catalysts.

Organic Synthesis Using Environmentally Benign Acid Catalysis Current Organic Synthesis, 2019, Vol. 16, No. 4 617

nanocomposite material was developed, in which the small Nafion-H particles are trapped in a porous silica network significantly enhancing both the BET surface and available active centers [31].

Metal-organic frameworks (MOF) [32] constitute a highly porous class of materials possessing an important internal surface area; thus they have found applications as gas storage media, and as absorbents but they also appear to be excellent catalysts. They have the particularity to be composed of organic linkers and inorganic metal ions [33]. Unlike zeolites that have a restricted number of structures, the hybrid nature of MOFs allows multiple combinations of both components yielding practically infinite structural possibilities. Various synthetic methods exist to prepare MOFs. The self-assembly approach is likely the most common: two solutions containing the organic and inorganic components, respectively, are mixed, often under solvothermal conditions that result in a crystalline framework [34]. Clusters of metal-carboxylates are common secondary building blocks acting as nodes in the MOF architecture. They come together to form a network linked by organic ligands such as terephtalic acid (Fig. 2). By selecting a particular ligands/metal cluster combination, the pore size as well as the flexibility of the material can be controlled and specific functionalizations can also be introduced. These easily tunable solid catalysts have therefore the potential to favor certain reactive intermediates and promote specific pathways, thus control the reactivity and selectivity of an organic reaction [35]. Moreover, the incorporation of chiral linkers extends the applications of the MOF to asymmetric catalysis [36].

Several composite materials are also often used solid acid catalysts. There are three major groups of catalysts that are particularly important in this area; the (i) carbon-, (ii) ionic liquid- and (iii) carbon silica composite based acids.

The first group is based on sulfonated carbon-based materials that were observed to be efficient and highly active solid Brønsted acid catalyst [38]. These catalysts resemble to graphite sheets that, after sulfonation, contain a high density of sulfonic acid groups. In fact the acid density of these materials surpasses that of Nafion-H by a factor of five. These materials are commonly prepared from susatinable sources, such as natural carbohydrates, e.g. starch, cellulose etc. by partial cabonization and sulfonation [39]. They are

used in a broad variety of applications for example metal-doped alternatives were applied in the Suzuki coupling and oxidation [40].

The ionic liquid-base composites in which ionic liquids are immobilized on solid surfaces, e.g. sulfonated silica also attracted significant attention [41]. These materials, such as ionic liquid coated sulfonated carbon-silica composites were found to be novel solid acid catalyst for aqueous phase organic synthesis [42].

Sulfonated carbon-silica composites are also important catalytic materials [43]. These catalysts have been applied in a variety of transformations, such as the Hantzsch cyclization [44], multi-component synthesis of heterocycles [45], the Michael addition of indoles to α,β-unsaturated ketones [46], chemoselective protection of aldehydes, and C, N, O-acylations [47].

Another new emerging class of solid acid catalysts is the nanoscale version of the polymer-supported acid catalysts (PSAs). The so called “nanoacid” corresponds to polymer-based nanoparticles functionalized with sulfonic acid groups [48]. A synthetic method reported the use of emulsion polymerization technique in presence of a reactive surfactant to prepare such material [48]. The co-monomers, styrene and divinylbenzene, employed were crosslinked under specific conditions in order to form a backbone of nanoparticles that remains heterogeneous in solution. The surfactant, octylbenzene sulfonic acid, possessing a benzenesulfonate moiety was then reacted with the particles depositing the sulfonic acid groups at their surface. The resulting material showed good performance in catalyzing the formation of urethane from isocyanate and alcohol. While nanoacid catalysts offer a greater surface area than PSAs and therefore possess a high potential to perform acid-catalyzed organic reactions, their success remain to be demonstrated as very few examples are available in the literature. It is interesting to note that the term nanoacid has been used for other materials, such as heteropolyoxometallate-based materials that possess nanometer size as well as strong acidic properties [49].

The last solid acid catalyst type discussed in this section is heteropoly acid salts, fundamentally different from the other types described previously. Heteropoly acids are made of hydrogen, oxygen, heteroatoms, and metals often including tungsten or molybdenum. In other words, they can be considered special clusters of transition metal oxides [12]. Heteropoly acids are

O O

O O

M OOO M O

OHO

HO O

HO O

OHO

HO O

OHO

HO O

OHO

organic linkersmetal cluster

Fig. (2). Representation of the synthesis of a metal organic framework with examples of metal cluster/organic linkers [37].


commonly soluble in water and many organic solvents. Their corresponding salts, obtained by replacing some or most of the hydrogens by large cations such as cesium, however, exhibit low solubility in both aqueous and organic media [50]. The resulting heteropoly acid salts have the potential to be recycled; they exhibit unique superacidic and multielectronic properties in addition to an important surface area when nanocrystallites are abundant within their structure. As a result they are interesting catalysts especially for acid or redox catalyzed reactions [51]. Their chemical composition can also be easily modified to adjust the desired redox and acid-base properties. The salts are often classified by the structure of the heteropolyanion that constitutes the fundamental unit called the primary structure. A secondary structure is generated by the connection of these heteropoly anions by hydrogen bonding. HPAs have been successfully used to promote alcohol dehydration, alkylation, esterification, polymerization and oxidation among other reactions [52, 53]. Despite their high acid strength however, some HPAs have a rather low surface area [54], which certainly is a drawback in heterogeneous applications.

The above short summary indicates that although the traditional solid acids, such as zeolites, clays or metal oxides (neat or sulfated) still dominate the field of solid acids, several new classes of these catalysts such as metal-organic frameworks, composite- materials and nanoacids have been developed to provide further variety and application possibilities for the traditional reactions and also allow the extension of the already broad scope applications.

2.2. Homogeneous Catalysis – Stable Soluble Acids

In its over two hundred years of history, homogeneous acid catalysis was successfully applied in a variety of transformations such as esterification, hydrolysis, aromatic electrophilic substitution and electrophilic addition, and many others. The traditional mineral acids, such as HCl or H2SO4 served as efficient catalysts for these reactions in the past. However, these acids are commonly highly corrosive, and many discharge poisonous fumes that represent safety and health hazards. The same is true for the conventional Lewis acids, such as aluminum chloride and bromide, or other metal-halogen compounds (TiCl4, SnCl4 etc.). These acids are all moisture sensitive, and decompose to metal oxides and hydrogen halides upon contact with water, whether it is during a reaction or a work-up procedure. In addition to the safety and health concerns this undesirable feature will also exclude the recycling of these catalysts and produce a significant amount of waste. Accordingly, significant effort has been made to replace these acids with greener alternatives both in industrial and laboratory applications. There are two major desired characteristics; (i) the acid should be stable under aqueous conditions and should not hydrolyze to allow recovery and recycling and (ii) it should have low vapor pressure in order to maintain a stable acid or catalyst concentration during a reaction and avoid toxic fumes. There have been several attempts on applying water soluble acids that do not hydrolyze under aqueous conditions and therefore are recyclable. The most typical examples are heteropoly acids [55] such as the commercially available H3[PMo12O40], H4[SiMo12O40], H4[SiW12O40], or H3[PW12O40]. These Keggin-type HPAs are soluble in water as well as in several organic solvents, and readily promote the typical Brønsted acid catalyzed reactions. However, due to their moisture insensitivity they can be regenerated from the reaction mixture upon removal of the solvent. The practical usefulness of HPAs generated extensive efforts in their synthesis and a large number of polyoxometallates have been prepared and applied for various purposes [56]. Another important group is that of trifluoromethanesulfonic acid (triflic acid) and its triflates [57], common salts of various metals, such as copper, gallium, lanthanides etc. and triflic acid that function as Lewis acids. In contrast to the traditional Lewis acids (such as AlCl3), these acids resist aqueous hydrolysis and can be recovered from such solutions. According to their properties, metal triflates

are well-known for forming complexes with organic ligands, thus opening a way for a broad range of applications including asymmetric catalysis [58]. However, due to their considerable cost, their widespread applications, particularly at the industrial scale, are not yet established.

The third large group of potentially sustainable acid catalysts is the acidic organocatalysts. These materials are organic compounds that possess considerable acidity and thus are capable of promoting acid-catalyzed reactions. Most of them, although not soluble in aqueous medium, are water tolerant and would remain stable during aqueous workup conditions. The traditional examples are alkyl or aryl sulfonic acids, such as para-toluenesulfonic acid (pTSA), that catalyze a variety of transformations [59]. Another such example, camphor sulfonic acid (CSA) extends the application of these acids to asymmetric synthesis [60]. Although, amino acids also possess weak inherent acidity and are often used in organocatalysis, the focus of the applications is not in acid-catalyzed reactions unless they are used as chiral ligands.

A new class of acidic organocatalysts, chiral phosphoric acids, was first reported in 2004, involving asymmetric organocatalytic Mannich reactions catalyzed by 3,3’-disubstituted (BINOL)-derived phosphoric acids [61]. These pioneering studies initiated extensive interest on the application of these unique compounds. Since their introduction, a large variety of transformations were carried out by chiral phosphoric acids, including Kabachnik-Fields, Pictet-Spengler, Strecker, Friedel-Crafts or Biginelli reactions, just to name a few [62].

The field of green soluble acid catalysts has been dominated by triflates and heteopoly acids on the past two decades. More recently, acidic organocatalyst were introduced and found exceptionally active and selective in a number of applications, mostly in the field of asymmetric catalysis. Although organo-catalysts are inherently green, their industrial applications are delayed by several factors. Among these, the often high cost (e.g. BINOL-based phosphoric acids), nearly stoichiometric amount required, and the difficult recyclability are the most detrimental issues that need to be addressed in future developments.

3. SYNTHETIC APPLICATIONS IN HETEROGENEOUS SYSTEMS

3.1. Friedel-Crafts and Related Reactions

The Friedel-Crafts reactions are one of the most fundamental transformations in organic chemistry. These processes are based on electrophilic aromatic substitutions and include acylation, alkylations, halogenation, nitration, sulfonation etc. Due to their practical importance the field has been the subject of numerous reviews and books, including Olah’s extensive series [63]. Despite the nearly one and a half century old history, Friedel-Crafts reactions are widely used in organic synthesis to create carbon-carbon bonds and therefore prepare useful substituted aromatic compounds [64]. The catalysts that were conventionally employed to perform such reactions are traditional Lewis-acids such as AlCl3 or BF3. They are used in stoichiometric quantities and consequently generate a considerable amount of toxic waste. In addition, the regioselectivity when using these catalysts is often rather poor [65]. Solid acid catalysts offer many advantages over the traditional Lewis acid catalysts in a typical Friedel-Crafts reaction. Unlike conventional Lewis-acids, they have been shown to efficiently catalyze these reactions with good recyclability and interesting selectivity.

Acylation. The role of common zeolites and their metal-doped counterparts was studied for the acylation of anisole with propanoic acid under solvent-free conditions (Scheme 1). The catalysts tested were ZSM-5 and BEA zeolites as well as their nickel, silver or iron-loaded derivatives [66]. Independently of the catalyst used, the


para- and ortho-products were predominant. The modified catalysts exhibited lower conversion compared to the original zeolites. This was explained by the replacement of Brønsted acid sites with Lewis acid sites that appeared to be detrimental for the reaction. The most efficient catalyst was found to be the pristine ZSM-5 zeolite yielding about 70% conversion and 80% selectivity. The same acylation could be carried out by MOF-based catalysts with high phosphotungstic acid loading [67].

Yadav and Kamble developed a new solid superacidic mesoporous UDCat-5 catalyst for the similar acylation of toluene with propionic anhydride [68]. The reaction occurred at 180°C, with relatively moderate yield (68%), however, with exclusive regioselectivity. The reaction was carried out under solvent-free condition.

Sulfated zirconia was found to be an efficient catalyst for the acylation of ferrocene with acyl chlorides, including long chain compounds such as heptanoyl chloride (Scheme 2). The reaction was carried out in dichloroethane under reflux conditions. The catalyst could be recycled in the reaction; five consecutive reactions resulted in no significant drop in activity and yields, in fact some activation (yield 88%) occurred during the subsequent reactions.

Alkylations. The microwave-assisted K-10-catalyzed alkylation and alkylation/electrophilic annulation of indoles were accomplished by using alcohols and diols as green alkylation reagents (Scheme 3) [69]. The alkylation with tert-butyl alcohol occurred with moderate to high yields with high selectivity toward

the C-3 position of indole. The solid acid appeared to show little sensitivity to the water that is eliminated during the reaction. Using 2,5-hexanediol the reaction occurred in a three steps sequence; alkylation, annulation and dehydrogenative aromatization to form 1,4-dimethylcarbazoles in good to excellent yields.

In a relevant extension, Cirujano et al. described a solvent-free Friedel-Crafts alkylation of indoles with alcohols (Scheme 4), avoiding the use of the often required organic solvents [70]. In particular, the performance of ionic liquids and solid acid catalysts (metal organic frameworks and zeolites) were compared in terms of activity, selectivity and reusability. The major conclusion of the study was that the ionic liquids provide the best activity but the microporous frameworks provided better recyclability and better selectivity. Given the importance of lowering the environmental impact, the microporous solids are of great interests. They also showed improved selectivity towards small mono-alkylated products. HY zeolites were found to be the most attractive option in terms of yield, cost and recyclability for this reaction.

Acidic cation-exchange resins were also employed to catalyze Friedel-Crafts-type reactions [71]. Thanks to their inherent Brønsted acidity, they are capable of catalyzing the formation of carbocations or other electrophiles essential for the occurrence of an aromatic electrophilic substitution. The commercially available and low-cost sulfonic acid resin D072 was used for the hydroarylation of styrene-derivatives and electron-rich arenes (Scheme 5). Under the optimized conditions the yields were close to quantitative with

O

HO

O

O

O

neat, 150 °C, 24 h

zeolite ZSM-5

55%

Scheme 1.

Fe + RCOCl

sulfated zirconiaFe

R

O

76 - 85%

C2H4Cl2, reflux, 4 h

Scheme 2.

NH

NH

CH3

H3C CH3

R

R

NH

R

H3C

CH3

K-10

MW

HO

HO

HO

130 oC

47-91%

52-96%

160 oC

Scheme 3.


selectivity in favor of the main isomer reaching 100% for some reagents or as low as 60% for some others. The activity of the selected resin was also investigated in a fixed bed flow reactor in order to evaluate its potential use in large-scale applications. The activity was maintained and the selectivity was improved compared to the batch conditions. While dichloroethane is not a green solvent, 100% atom economy, the green alkylating agent and the recyclable catalyst substantially compensate this disadvantage.

The well-known, perfluoroalkyl-sulfonic acid resin Nafion-H served as a catalyst in the preparation of triarylmethanes from benzaldehydes and arenes under microwave irradiation and solvent-free conditions (Scheme 6) [72]. The combination of the solid acid catalyst and the activation method proved to be effective to produce high yields in short reaction times. Different regioselectivities were obtained depending on the activation methods: microwave irradiation favored the formation of ortho-ortho products while conventional heating mostly yielded para-para products. The obvious advantages of the method lie mainly in the nature of the catalyst that is environmentally friendly and can be filtered off for an easier product separation, as well as in the use of a green alkylating agent, that only produces water as byproduct. However, the recyclability of the catalyst was not investigated.

A similar process has been developed for the synthesis of bis(indolyl)methanes via the alkylation of indoles with aldehydes (Scheme 7). According to the significantly enhanced reactivity of indoles, the inexpensive and abundant catalyst SiO2 could be used under solvent-free conditions [73]. The reaction showed a broad substrate scope using a variety of aromatic aldehydes all providing high yields. Although the highest yields were obtained with silica as a catalyst, the reaction was not catalyst specific. The similarly abundant and inexpensive acidic Al2O3 was also found to be an effective catalyst for the reaction, however, resulting in slightly lower yields.

Due to its significant acidity and high surface area, K-10 montmorillonite is a widely used catalyst for various transfor-mations including the Friedel-Crafts reaction. As shown in Scheme 8, K-10 efficiently catalyzed the alkylation of indoles and pyrrole with nitroalkenes under solvent-free conditions at moderate temperature (60°C) providing high yields [74]. In addition to the low cost and environmentally benign nature of the catalyst, it appeared recyclable during three consecutive cycles.

Several works have exploited the catalytic potential of non-conventional biomass, such as metal hyper-accumulator plants, in

NH

H

NH

4%mol HY zeolite

H3CO

OHOCH3

up to 90%

neat, 50 °C, 2-8 hR

R

Scheme 4.

R

R

Ar

ArH30wt% D072

reflux in DCE, 4h

81-100%0-60:100-40

Scheme 5.

O H

R1 R2

Nafion-H

R1

R2

R2R1

R1

+

21-100%

neat, 150 °C, 25-190 min

MW or conventional heating

Scheme 6.

O

R1

HN

SiO2 or Al2O3 (acidic)

MW, 90 ˚C, 5-15 min

HN NH

R1

59-98%

2

R2

R2R2

Scheme 7.


combination with the same common porous support, mon-tmorillonite K-10 [75]. Grison et al. demonstrated the clear advantages of heterogeneous catalysts over their homogeneous counterparts [76]. The heterogeneous plant-based Lewis acids afforded high yields and good recyclability with consistent yields for up to four consecutive cycles. Two reactions were studied: the acylation of anisole with acetic anhydride and the alkylation of aromatics with alkyl halides (Scheme 9). The combination of Zn hyper-accumulative plants supported on K-10 was demonstrated to be the most efficient catalyst providing yields ranging from 50% to 100% depending on the reactants. In addition, the results obtained with these ecocatalysts were considerably superior to the results obtained with the commercial Lewis-Acid ZnCl2.

Numerous examples have shown the performance of metal organic frameworks in Friedel-Crafts reaction as well. They often are functionalized in order to improve their performance. Urea-containing MOF have recently attracted attention for the alkylation of indoles with nitroalkenes. Urea-based compounds are known for their capacity to participate in hydrogen-bonding and therefore act as organocatalysts. In traditional homogeneous systems, they undergo self-quenching and consequently require high catalyst loading. Functionalizing MOFs with urea moiety yielded interesting

results. Luo et al. synthesized a MOF from V-shaped dicarboxylate ligands and dicopper units [77]. The obtained simple 2D structure was believed to ease the access of the substrates while stabilizing the urea moieties, previously attached to the building blocks. The resulting heterogeneous catalyst was highly active in the Friedel-Crafts alkylation of indoles with nitrostyrene (Scheme 10); it was tolerant towards various substituents and exhibited good recyclability. Another similar study reported the alkylation of indoles with various nitroalkenes catalyzed by a zinc-based MOF containing ureylenic acid as the hydrogen-bond-donor [78]. The authors also observed a significant increase in activity upon heterogenization of the urea organocatalyst. When employed as catalysts for Friedel-Crafts reactions, the desired products were obtained in high yields in toluene at 60°C.

The synthesis of a large number of organofluorine indole and pyrrole derivatives was achieved by a K-10-catalyzed aromatic electrophilic hydroxyalkylation (Scheme 11) [79]. Several of the synthesized products showed good to excellent activity in the inhibition of the fibril formation of Alzheimer’s disease’s amyloid beta peptide [80].

Halogenations. The chlorination of aromatic compounds was performed using various types of zeolites. One of them, the proton-

Ar

NO2

NH

Ar

NO2NH

R

neat, K-10, 60 °C,15-75 min

RNH

neat, K-10, 60 °C, 20-35 minNH Ar

O2N

81-94%84-93%

Scheme 8.

R1

R2 X R2 H X

Zn-hyper-accumulative plants/ K-10

52-100% o/m/p: 15-30/0/85-70

neat, RT, 1 h

R1

Scheme 9.

R3NO2

N

R4

N

R3NO2

R4

toluene, 60 °C, 24 h

Zn-MOF-urea

R1NO2

NH

NH

R1NO2

Cu-MOF-urea

acetonitrile, 60 °C, 18 h

R2R2

81-98%

80-92%

Scheme 10.


exchanged zeolite X, catalyzed the chlorination of toluene at ambient temperature in different solvents using tert-butyl hypo-chlorite (Scheme 12) [81]. The solvent effect appeared to be an important factor for the selectivity as well as the conversion. The best results in terms of both yield and selectivity were obtained in ether, probably due to its polarity that is believed to stabilize the oxonium intermediate and aid the selectivity. Tetrachloromethane also provided high yields; however, both solvents cause many health and environmental issues.

zeolite/tert BuOCl

Et2O, RT, 1 h

Cl

60%

Scheme 12.

Mohan et al. reported a regioselective bromination reaction using the widely-used montmorillonite K-10 clay in presence of N-bromosuccinimide (Scheme 13) [82]. Various aralkyl ketones were converted to α-monobrominated aralkyl ketones in methanol at mild temperature (65°C) with excellent yields and short reaction times. In addition to the simplicity and the efficiency of the method, the reusability of the catalyst is another benefit of the method surpassing other existing procedures that suffer from disadvantages such as the use of toxic brominating agents, long reaction times or tedious workup.

O

R

O

BrM-K10/NBS

Methanol, 65 °C, 10-20 min

R

45-95%

Scheme 13.

Nitration: Several works have reported successful nitration of aromatics over zeolites in attempts to substitute the concentrated acidic solution mixture (nitric and sulfuric acids) that is tradi-tionally employed for this reaction type. For instance, the nitration

of phenol over the acidic zeolite Hβ in ethanol resulted in a combined yield of 86% with a para/ortho ratio approaching 1 (Scheme 14, a) [69]. Although the regioselectivity could be imp-roved by using hexane instead of ethanol, selecting this solvent is not in favor of the environmental impact. In addition, the method doesn’t completely eliminate the use of acidic solutions since a dilute solution of nitric acid was still used as the nitrating agent. Another work employed similar zeolites in dichloroethane under reflux for 48 h (Scheme 14, b) [69]. It was observed that the best results were obtained when zeolites had large pores to optimize the reaction rate and restrictive channel structure to better control the regioselectivity. While the combined yield was lower than for the first method, the selectivity was higher. This method used isopropyl nitrate, another nitrating agent.

Kumar et al. reported the nitration of aromatics with silica supported perchloric acid or bisulfate under solvent-free micro-wave-driven conditions (Scheme 15) [83]. The green nitrating agent NaNO2 in combination with the supported acidic catalyst yielded excellent results in short reaction times. Perchloric acid was preferred over bisulfate due to its low nucleophilicity and higher acidity. The catalyst was easily prepared and could be reused for four consecutive cycles.

X

NO2

X

silica supported HClO4 or HSO4/NaNO2

MW, 1-4 min

70-82%

Scheme 15.

3.2. Condensations

Condensation reactions, an acid or base-catalyzed sequence of an addition and an elimination reactions, are versatile and constitute a broad scope of transformations that enable the synthesis of a wide range of products [84].

The K-10–catalyzed microwave-assisted condensation of substituted aryl trifluoromethyl ketones and different primary amines yielded the corresponding trifluoromethyl imines (Scheme 16) in good to excellent yields. Although most of the reaction conditions qualify as green, high temperature (175°C) and somewhat long reaction times (45-60 min) were required even with

N

toluene, K-10, 60 °C, 15-75 min

N

toluene, K-10,60 °C, 20-35 min

86-98%

R2

R1

R3

R4

R5

R6

F3C

O

COOEt

n N

R4

R5

R6

NR2

R1

R3F3C OH

COOEt

nCF3

OH

COOEt

n

80-98%

Scheme 11.

OH

NO2

NO2

OH OH

a. EtOH, dilute HNO3 RT, 2 hb. DCE, isopropyl nitrate, reflux, 48 h

44:4240:13

zeolite

Scheme 14.


microwave activation to counter the low reactivity of the trifluoromethyl ketones. Despite the relatively harsh conditions the K-10/microwave protocol was still significantly greener than a similar, conventionally heated process that was catalyzed by PTSA; for some reactants as long as 7 days of heating at 175°C was needed to achieve 70-80% yields. The K-10 catalyst could be reused without any loss of activity [85]. The method could be successfully extended for the synthesis of chiral amines by carrying out the condensation with enantiomeric methyl-benzyl amines and hydrogenate the imines to secondary amines and finally remove the benzyl group by hydrogenolysis [86].

Chalcone derivatives were synthesized via the aldol con-densation of acetophenones and benzaldehydes. The process was catalyzed by boric acid and was carried out under microwave-assisted solvent-free conditions (Method A) [87]. Due to the low solubility of boric acid, the reaction occurred in a rather hetero-geneous system and the products were obtained in medium to good yields. The chalcones were obtained as the E stereoisomer with almost exclusive selectivity and were isolated in a pure form after a simple extraction of the product mixture (Scheme 17, Method A). In a very similar approach (Method B) KSF montmorillonite was used as a catalyst [88]. The products were obtained in medium to good yields. Electron withdrawing substituents appeared to negatively affect the yield. (Scheme 17, Method B).

Acidic ion exchange resins, such as Amberlite IR 120H, were also found to be excellent catalysts for the condensation reaction of aryl aldehydes and hydroxylamines (Scheme 18) [89]. The solvent-free reactions provided high yields in short reaction times. The ion exchange resin could be readily recycled with only a negligible drop in activity even after the fourth consecutive run. The reaction

appeared to be surprisingly substrate tolerant; a broad group of benzaldehydes was subjected to the experimental conditions without significant changes in yield.

3.3. Multicomponent Reactions

The concept of multicomponent reactions is very simple; a cascade of reactions occurs in a specific order in one pot by simply adding the reactants to the reaction mixture at the beginning of the reaction producing a well-defined product selectively. This way, large compounds of complex structure can be prepared without the need of several purification steps of intermediates thus saving time, energy and effort, while also avoiding the formation of a potentially large amount of chemical waste. Therefore, multicomponent reactions are particularly attractive for green synthesis [90]. Given their attractive features these reactions have a long history dating back to the classic Hantzsch or Biginelli reactions from the late 1800s. Newer applications such as the Ugi reaction reinvigorated this field in the late 1950s.

The traditional Hantzsch synthesis was successfully modified to an even greener heterogeneous catalytic approach by using a simple physical mixture of Pd/C and K-10 montmorillonite. The use of this catalyst mixture is a typical example of bifunctional catalysis. The solid acid K-10 efficiently catalyzed the condensation and cyclization of aldehyde, ethyl acetoacetate and ammonium acetate to result in typical Hantzsch esters. The successive dehydrogenative aromatization of the intermediate was catalyzed by the noble metal component to yield pyridine derivatives in moderate to excellent yields (Scheme 19) [91].

MW, 175 oCR1 CF3

O

+R1 CF3

NR2

53 - 95%

R2 NH2

K-10

2. debenzylation

1. H2/cat

R1 CF3

NH2

Scheme 16.

B(OH)3 (20mol%)MW, 160 ˚C, 40 min

58-75%

O

O

R1 R2

O

R1 R2

Method A

Method BKSF montmorillonite,MW, 150 ˚C, 60 min

43-97%

Scheme 17.

Amberlite IR 120H

MW, 120 W, 2-3 min

75-85%

O

R

N

R

H2NOH . HCl

Scheme 18.


A similar, K-10-catalyzed microwave-assisted approach was developed for the synthesis of quinolones by a three component reaction using anilines, aldehydes and terminal aryl alkynes (Scheme 20) [92]. The reaction pathway is of domino nature; the first step is the formation of an imine between the aldehyde and the aniline, which is immediately followed by the intermolecular addition of the triple bond to the imine. This intermediate then undergoes cyclization. Although the above steps are catalyzed by the strong acid centers of K-10, the last step, the oxidative aromatization, is due to the mild oxidative properties of this catalyst that is common to other montmorillonites as well.

The preparation of substituted pyrroles was achieved by Jeong et al. using a four-component reaction [93]. The authors reacted a β-ketoester, an amine, an aldehyde and nitromethane in the presence of catalytic amount of p-toluenesulfonic acid doped polystyrene (PTSA-PS) (Scheme 21). The microwave irradiation resulted in high yields in short reaction times as compared to conventional heating. The catalyst was reused in seven consecutive reactions with only a negligible loss in activity.

3.4. Couplings

The traditional coupling reactions, such as the Heck, Suzuki or Negishi couplings are typical metal-catalyzed reactions [94]. Since their original discoveries the field has enjoyed considerable success [95] resulting in the Nobel Prize for the three scientists [96]. Thus acid-catalyzed approaches are relatively rare and occur through a different mechanism.

An environmentally benign metal-free, K-10 montmorillonite catalyzed domino-style approach was developed for the direct synthesis of biaryls by solid phase diazotization of anilines and successive nucleophilic attack by aromatic hydrocarbons that led to C-C bond formation (Scheme 22) [97]. The reaction provided excellent yields using a broad range of substituted anilines and a variety of aromatic nucleophiles. The catalyst was found to be recyclable five times without a notable loss of activity.

NH2 NaNO2, K-10

110 oCR1 R2

R1

R2

58-98% �Scheme 22.

3.5. Rearrangements

Rearrangements are useful transformations to obtain compounds that are difficult or tedious to obtain in a direct route. Solid acids such as zeolites played an important role in early rearrangements in the chemical, particularly in the petrochemical industry, serving as catalysts for alkene isomerization or cracking reactions.

The superacidic Nafion-H and Nafion SAC-13 were found to be effective solid acid catalysts for the synthesis of trifluoromethyl

R

H O

O

O

O

O

O

O

NH4OAc

Pd/C/K-10

N

R

EtOOC COOEt

H3C CH3MW, 130 oC

45-95%

Scheme 19.

R1

NH2CHO

N R1R2

R2

R3

R3

70-96%

K-10

MW, 100 oC

Scheme 20.

NH2

CHO

MW, 80 ˚C, 51-66 min

R4

R3

R1 OR2

OO

NO2 NR1

O

R2O R4

R3

PTSA-PS

Scheme 21.


ketimines from benzylamines and trifluoromethylated ketones (Scheme 23) [98]. The reaction occurs via a condensation and a subsequent benzylimine-benzaldimine rearrangement via a facile 1,3-hydrogen shift. The reaction can be carried out under a wide range of reaction conditions such as microwave irradiation and flow system. It appeared that with the appropriate selection of the temperature one could direct the reaction to form the simple Schiff-base (164°C) or the rearranged benzaldimine (185°C) as major products. As the major goal of this work was to synthesize aldminines via the rearrangement, the initial step toward the formation of the benzylimine was not investigated separately and yields were not determined.

Ar NH2 + R CF3

ONafio

n-H

Nafion-H

164 o C

185 oC

Ar N CF3

R

Ar N CF3

R

36-94% �Scheme 23.

3.6. Ring Transformations

Ring transformations include cyclization as well as ring-opening reactions, both are important synthetic tools [99].

Cyclizations: The above described Pd/C/K-10 bifunctional catalyst was applied in the microwave-assisted synthesis of pyrazoles from chalcones and hydrazines. The concept was also similar to those mentioned above, K-10 catalyzed the condensation and subsequent cyclization, and the Pd promoted the last dehydrogenation/aromatization step. A broad variety of hydrazines and chalcones were applied to assess the scope of the method. The products were obtained in good to excellent yields (Scheme 24) [100].

Phthalaldehydic acid (2-carboxybenzaldehyde) served as starting materials for the synthesis of valuable products. Its K-10 montmorillonite-catalyzed reaction with methylaryl and cyclic ketones yielded isobenzofuran-1(3H)-ones in excellent yields (90-98%) via condensation and successive lactonization reactions (Scheme 25) [101]. A similar reaction using aryl-hydrazines led to the formation of phthalazinones by forming a hydrazone intermediate that immediately underwent cyclization (Scheme 25) [102]. The application of microwave irradiation substantially increased the reaction rates in both reactions and the products formed in short reaction times (1-40 min).

The synthesis of a broad variety of N-acyl-indoles and sulfonyl-pyrroles was completed by the cyclization of 2,5-dimethoxy-tetrahydrofuran with amides [103] or sulfonamides and amines [104] by microwave-assisted K-10 catalysis (Scheme 26). The product N-sulfonyl-pyrroles were found to be effective (IC50=32-135 nM) inhibitors of the FBPase enzyme, and thus could be considered as drug candidates for type 2 diabetes [105].

The synthesis of benzimidazoles, benzodiazepines, quinoxali-nones was achieved by a solvent-free microwave-assisted K-10 montmorillonite-catalyzed method. A variety of substituted o-phenylenediamines readily reacted with ketones, aldehydes and bifunctional reagents to form the products (Scheme 27) [106]. The bicyclic condensed heterocycles were obtained in moderate to excellent yields (53-99%) and excellent selectivities in short reaction times (mostly 1-10 min).

The synthesis of β-carboline-core based drug candidates was achieved by a Pd/K-10-catalyzed microwave-assisted Pictet-Spengler cyclization of substituted tryptamines with various aromatic aldehydes and glyoxals (Scheme 28) [107]. The reaction proceeded by the acid (K-10)-catalyzed formation of an imine between the tryptamine and the carbonyl compounds and the subsequent cyclization to the tetrahydro intermediate. The additional Pd content of the catalyst completed the process by catalyzing the oxidative dehydrogenation/aromatization step. The compounds were found to be excellent inhibitors of amyloid-beta oligomer formation and butyrylcholinesterase activity, and also showed moderate anti-fibril properties [108].

O

R1

R2

NH2

HNR3

NN

R3

R1

R2Pd/C/K-10

MW, 160 oC, 20-30 min

Yield: 80-98%

Scheme 24.

OH

H

O

O

NH2

HNR4

N

N

R4

OK-10, MW, 100 oC

59-98%

R1

K-10, MW, 170 oC

R3

R2

O

O

O

R2

R1

OR1 R1

90-98%

Scheme 25.


A similar approach was applied for the K-10-catalyzed microwave-assisted synthesis of quinolines from anilines and cinnamaldehydes (Scheme 29) [109]. Reactions were completed in a matter of minutes and although mostly excellent yields were obtained, substrates with potential electron pair donor substituents, such as methoxy, only resulted in moderate yields, likely due to a complexation with the Lewis acid centers of the catalyst.

The microwave-assisted solid phase diazotization of o-phenylenediamines with K-10 montmorillonite appeared to be a

novel method for the synthesis of 1,2,3-benzotriazoles (Scheme 30) [110]. The method was based on a sequence of reactions that was initiated by the acid centers of K-10, namely the production of nitrous acid that reacted with the amino group of the phenylene-diamine. Once the nitroso intermediate formed it underwent an immediate ring closure with the other NH2 group due to their close proximity forming the benzotriazoles. The reaction showed broad applicability providing high yields for all substrates used.

K-10, MW, 80 oC

Ar N

O

Ar-C-NH2

O

R-NH2

K-10, MW, 100 oC

N

R

K-10, MW, 100 o C

N

SO2Ar

ArSO2NH2

85-92%

83-95%

60-85%

OH3CO OCH3

Scheme 26.

NH2

NH2

R

R1 CHO

R3

O

K-10, MW

K-10, MW

R

N

N

R1

R

R1

NH

N

R3

R3

R2

R2

R2

R4

O

O

O

NH

N

O

R4

RK-10, MW

75-99%

78-95%

53-99%

Scheme 27.

NH

NH2

+

O

H Ar

Pd/C/K-10

MW, 130 C NH Ar

NH

NH Ar

N

tetrahydro-β-carboline β-carboline

R RR

71-96%

Scheme 28.


The K-10-catalyzed microwave-assisted 5-exo-dig cyclo-condensation of alk-3-yn-1-ones with hydrazines led to the successful synthesis of diversely substituted pyrazoles (Scheme 31) [111]. The combined application of the clay-based solid acid and microwave irradiation allowed the elimination of organic solvents during the heating and the products were obtained in excellent yields. Due to the different reactivity of the carbonyl group and the triple bond the reaction occurred with exclusive selectivity.

Several K-10-catalyzed cyclization reactions were assessed regarding their energy efficiency comparing microwave-assisted and conventionally heated examples. Six reactions were compared using the normalized energy consumption. It was found that the microwave activated ones were more energy efficient than the traditional counterparts in five of the six reactions. However, the one example when the traditional heating was more energy efficient indicates that every reaction should be individually assessed for energy efficiency, and the green label should not be automatically applied for microwave-assisted synthesis [112].

Cu triflate catalyst was successfully applied for the synthesis of fused chromenopyridines. The reaction has been performed under green conditions, using air as oxidant in a solvent-free system [113]. Due to the favorable redox properties of Cu, the Lewis acid catalyzed the Michael-addition as well as the final oxidation of the intermediate to the product (Scheme 32). Although the intermediate underwent aromatization even in a catalyst free system, the yield and reaction rate improved significantly when the catalyst was present providing excellent yields.

The solvent-free Pechmann condensation was applied for the preparation of coumarins via an acylation-cyclization sequence of phenols with methyl acetoacetate using zirconium(IV) phospho-tungstate (ZrPW) as a solid acid catalyst [114]. The expected products were obtained in short reaction times, albeit in moderate yields (Scheme 33). The catalyst appeared to be recyclable, although it required an acid recovery treatment to restore its catalytic activity. A similar study applied Envirocat EPZ-10 as a catalyst for this reaction [115]. Although the conditions were about

NH2

R1

R3

O

R4

+

MW, 90 oC N

R1

R3

R4

R2R2

55-95%

K-10

Scheme 29.

NH2

NH2NH

N

NNaNO2

K-10, MWR

92-99%

R

HN

NH2

R

N

O

Scheme 30.

Ar1

Ar2

+

O

NH2NH RMW, 100 oC

NN

Ar1

Ar2

R

73-91%

K-10

Scheme 31.

O O

R1

NH2

R2

O

EtO2CCu(OTf)2 (10mol%), air

MW, 90 ˚C, 15-35 min

O O

R1

N

R2

CO2Et

70-93%

Scheme 32.

OHR

O

OMe

O

MW, 130 ˚C, 30 min

ZrPW

OR

O

54-66%

Scheme 33.


the same, the new catalyst appeared to make a significant difference and resulted in good yields.

The successive ring opening-cyclization of epoxychalcones in the presence of montmorillonite KSF under microwave-assisted solvent-free conditions resulted in the formation of flavonols (Scheme 34) [116]. A broad scope of different aromatic substituents was tolerated and the formation of the products occurred in excellent yields in very short reaction times.

Aziridines are versatile synthetic building blocks that are used in highly regio- and stereoselective ring-opening reactions. K-10 montmorillonite has been applied as a catalyst for the synthesis of aziridines in a simple, ambient temperature approach using imines and ethyl diazoacetate as starting materials (Scheme 35) [117]. The reaction resulted in the formation of cis-aziridines. The solid, easily recyclable catalyst, the short, room temperature reactions, the high atom economy, the excellent yields (90%) and exclusive selectivity all point toward an excellent example of sustainable synthesis.

N

Ar2

Ar1+ N2CHCO2Et

K-10N

CO2Et

Ar1

Ar2

RT

74 - 91% �Scheme 35.

A microwave-assisted aminolysis of epoxides was catalyzed by BiCl3 on SiO2, an efficient heterogeneous catalyst. The reaction readily provided β-amino alcohols in high yields under solvent free conditions [118]. The catalyst could be recycled for five times without loss in activity. The microwave activation enhanced the yields even under shorter reaction times compared to conventional heating. A broad variety of epoxides could be successfully applied with negligible substituent effect (Scheme 36).

Acids have been proven to serve as effective catalysts for the ring-opening reaction of lactones as well. As acidic conditions are also likely to catalyze the reverse reaction, i.e. lactone formation, the ring opening often is only successful if an immediate subsequent reaction is involved further transforming the primary product hydroxy-acids. In a recent study, Zhu et al. showed that metal triflates can be efficient in the ring-opening-hydrogenolysis of lactones to produce the corresponding carboxylic acids (Scheme 37) [119]. While several different metal triflates were effective in

the reaction, tungsten was found to be the most active. The metal cation acts as a Lewis-acid in both the ring-opening polymerization as well as the depolymerization forming an unsaturated acid that is then reduced by a conventional Pd/C catalyst. A broad range of different sized lactones could be transformed under relatively mild conditions and in mostly high yields.

25-96%

H2, neat, 135˚CO

O

R

nHO

O

Hn

RPd/C (0.5mol%), W(OTf)6 (2mol%)

Scheme 37.

Gowda and Chakraborty used the environmentally benign Lewis acid FeCl3 as catalyst for the ring-opening polymerization of lactones (Scheme 38) [120]. The reactions gave full conversion to the polymer and good molecular weights of the polymers were obtained. The molecular weight distribution was shown to be superior to that obtained with other more complex iron catalysts.

100%

toluene, 27˚CO

O

nHO

O

OHn mm

FeCl3

Scheme 38.

Similar reactivity was obtained for the ring-opening polymerization of β-butyrolactone and lactide using a zinc-amine complex [121]. Miller et al. demonstrated that the Sb2O5 is effective in catalyzing the ring-opening polymerization/poly-condensation reaction between lactones and aromatic hydroxyacids [122]. The products were obtained in high yields and good molecular weights.

3.7. Asymmetric Synthetic Applications

The most common way to design heterogeneous catalytic applications is to immobilize either a chiral modifier on the surface of a solid catalyst or a chiral catalyst (e.g. metal complex) on the surface of a catalyst support.

The group of Freire and Pires showed that the asymmetric epoxidation of styrenes was possible under heterogeneous conditions using a manganese (III) salen complex immobilized on

montmorillonite KSF

MW, 120 ˚C, 2-3 min

90-96%

O

O

S

O

Ar O

O

Ar

OH

O

O

Scheme 34.

O

R1

H2N

R2 MW, 15 min

BiCl3/SiO2

84-100%

HO

R1

NH

R2

Scheme 36.


functionalized porous clay heterostructures (PCHs) [123]. The thus prepared catalyst enabled to obtain the desired epoxides in high enantiomeric excess but only in low yields (Scheme 39). While the method is attractive due the use of a heterogeneous catalyst and the high enantioselectivities obtained, the use of dichloromethane as solvent and the non-recyclability of the catalyst limit the performance with regard to green chemistry metrics.

DCM, 0 ˚C

Mn(III)-salen-PCHmCPBA / NMO

16-57%79-100%ee

R2

R1

R2

R1

O

Scheme 39.

Lin et al. used a chiral metal-organic framework (CMOF) containing Mn-salen unit as linker for the asymmetric epoxidation of cyclic alkenes [124]. By generating isoreticular MOFs with different cavity size the authors observed that the epoxidation rate was clearly dependent on the channel dimension. While the catalyst could be recycled for up to 4 times without loss of activity and enantiomeric excess, the reaction suffered from the need of dichloromethane as solvent and 2-(tert-butyl-sulfonyl)iodosyl-benzene as oxidant (Scheme 40).

Similar results were obtained by Huang et al. using a Jacobsen’s type catalyst bound to zirconium poly(styrene-phenylvinylphosphonate)-phosphate (ZPS-PVPA) and mCPBA/ NMO as an oxidizer [125]. The reactions proceeded with high yields and enantioselectivities and the catalyst was reused for up to seven times without notable loss of activity and enantioselectivity. The authors showed that the reaction performed well on a large scale using the same procedure giving identical yields and enantioselectivities. Dichloromethane, used as the solvent for the reaction, however, led to an increase in the environmental impact of the reaction.

Using a CMOF containing a Ni-salen moiety as catalyst the insertion reaction of carbon dioxide into propylene oxide was possible [126]. The reaction used racemic propylene oxide as starting material and did not require the use of a solvent (Scheme 41). Although the enantioselectivities obtained were moderate and

the conversion was low, this method represents an interesting new procedure for a chiral resolution reaction.

ONi-salen-CMOFNBu4X

CO2 (2MPa)

OO

O

16-86%8-52%ee �

Scheme 41.

The sequential one-pot asymmetric epoxidation-ring-opening reaction of alkenes was shown to be effectively catalyzed by a multivariate MOF [127]. The MOFs used contained salen units with different metal ions as active centers. A variety of nucleophiles was used in the ring opening and the products were generally obtained in high yields and regio- as well as enantioselectivities (Scheme 42). As described previously, 2-(tert-butyl- sulfonyl)iodo-sylbenzene was used as the oxidant and dichloromethane as solvent which significantly increases the environmental impact of the reaction.

Jiang and co-workers showed that a porphyrin-salen based MOF can be used as a catalyst in the asymmetric cyanosilylation of aldehydes (Scheme 43) [128]. The reaction provided the desired products with moderate to high yields and enantioselectivities. The easy product separation and recyclability of the catalyst are negatively counterbalanced by the use of stochiometric amounts of PPh3O as an activating agent and the use of dichloromethane as a solvent.

Cui et al. used a chiral porous organic framework (POF) functionalized with Rh as Lewis acid catalyst for the asymmetric conjugate addition of arylboronic acids to unsaturated ketones [129]. A variety of enones and arylboronic acids were coupled in mostly high yields and enantioselectivities (Scheme 44). The catalyst was easily recovered by centrifugation and could be reused for five consecutive runs without significant loss in activity and enantioselectivity. The environmental impact of the reaction is increased by the fact that 50 mol% KOH have to be added and the reaction needs to be run in a dioxan-water mixture. The authors also demonstrated that the chiral POFs can be used as a separating agent in chromatography.

DCM, RT

Mn(III)-salen-CMOF

54-99%39-92%ee

R R

O*

*SO2tBu

IO

Scheme 40.

DCM, 0°C

75-94%85-99%ee

R R

SO2tBu

IO

MTV-MOF+ NuH

OH

Nu

Scheme 42.

DCM, -20°C

1% ps-MOFPPh3O

42-96%55-98%ee

O

R

OTMS

R

+ TMSCNCN*

Scheme 43.


3.8. Oxidation of Alkenes

The oxidation of alkenes is traditionally performed by using organic peroxides or inorganic metal oxides in high oxidation states, both systems producing a large amount of low-value byproducts. To overcome this issue the use of solid acids in combination with environmentally friendly oxidizing agents such as hydrogen peroxide or oxygen has been explored. Xia et al. used 30% H2O2 and a solid phosphotungstic acid catalyst for the epoxidation of cyclohexene (Scheme 45) [130]. The catalyst was prepared by simple exchange reaction with an anion-exchange resin and performed the desired reaction in high yields and selectivities. The catalyst could be recycled for up to five times without losing activity and selectivity. The authors also demonstrated that the scope could be extended for other substrates but with decreased yields and selectivities.

35-98%

CH3CN, 50°CO

n n

D201-PWAR(4), 30% H2O2

Scheme 45.

In a very similar approach the same group used a polystyrene-bound peroxophosphotungstic acid as a catalyst for the epoxidation of various dienes with H2O2 [131]. The best results were obtained with dicyclopentadiene where the monoepoxide was obtained in nearly quantitative yield. The catalyst could be recycled for up to eight times without losing activity.

The solid acid KSF montmorillonite successfully catalyzed the aqueous phase oxidative cleavage of styrenes to benzaldehyde with air, in a process that can be viewed as an environmentally benign alternative to ozonolysis (Scheme 46) [132]. Although the reaction showed high selectivity and conversion in the oxidation of styrene, the cleavage of substituted derivatives occurred in lower yields and selectivities. The Fe-content of the catalysts was proposed as a

major contributor to the mode of action, although the acid centers played a role in the cleavage of the intermediates.

3.9. Miscellaneous Reactions

It appears that acidic montmorillonites possess properties that allow them to serve as mild oxidation catalysts as well. K-10 montmorillonite successfully catalyzed the partial oxidation of benzylamines to benzaldehydes and the immediate successive condensation of the product benzaldehydes with the excess amine to form benzylidene-benzylamines. Using a mixture of benzyl-amines and anilines mixed products, e.g. benzylidene-anilines were also obtained in excellent yields (Scheme 47) [133, 134].

A tailored catalyst, methanesulfonic acid deposited on Al2O3, was applied in the esterification of carboxylic acids in a solvent-free, microwave-assisted process [135]. The scope of the reaction was broad; a variety of aromatic and aliphatic acids could be esterified with common alcohols. The process provided high yields in short reactions (Scheme 48) and could be extended to the esterification of α-aminoacids.

Solid acids have also been applied in the degradation and transformation of natural saccharides using a variety of these materials [136]. For example a patented method proposed a highly effective polymerization of building blocks derived from unlimited resources such as glycosides, employing solid superacid catalysts [137]. The method consists of reacting the starting materials with sulfonated metal oxides, such as sulfonated iron oxide or zirconia sulfate, by a melt polymerization or a solution polymerization process. For instance, D-glucose was polymerized without solvent in an electric furnace using an equivalent amount of sulfated zirconia at a temperature corresponding to the melting point of the saccharide for 24h. The method allowed the production of multiple polymers of saccharides in one simple step making the procedure relatively environmentally friendly compared to the wasteful multi-steps traditional methods.

O

+ ArB(OH)2

O

Ar

4mol% POF-Rh50mol% KOH

1,4-dioxan/H2O, 50°C

55-93%40-93%ee

Scheme 44.

R OH

O

HO

n MW, 80-120 ˚C, 8-20 min

CH3SO3H/Al2O3

R

O

O n

69-98%

Scheme 48.

KSF-montmorillonite

H2O, 70 oC

O

R2

R3

R1

R2

R1 25-89% �Scheme 46.

NH2

NMW

K-10, 150 °C

R1

R1 R1

N

MW

K-10, 140 °C R1

+

NH2

R2

R2

NH2R1

+

76-98%

79-98% Scheme 47.


The above subchapter gives an overview of the many application possibilities of solid acids in synthetic processes. A wide variety of approaches are described. Essentially, solid acids can be applied and thus can replace harmful mineral acids in every process that has been attempted by traditional acid catalysis. It is widely believed that these materials are the future of acid catalysis and accordingly the development of the field is rapid and extensive. In addition to the common solid acids, such as clays, zeolites and acidic ion-exchange resins, several new classes of materials were introduced to the field and helped extending applications and will have a great impact on upcoming developments of new and potentially greener processes.

4. SYNTHETIC APPLICATIONS IN HOMOGENEOUS

SYSTEMS

4.1. Friedel-Crafts and Related Reactions

The major goal in contemporary, sustainable homogeneous Friedel-Crafts chemistry is to replace the traditional catalysts, such as mineral acids and moisture sensitive Lewis acids with water stable recyclable acids.

Acylation: Metal triflates are one of the most popular green acid catalysts in homogeneous catalytic applications. Anisole derivatives were acylated with acetic anhydride using Sc(OTf3) and a dendritic

terpyridine ligand as the catalyst (Scheme 49) [138]. The appli-cation of microwave heating ensured short reaction time when derivatives with strong electron withdrawing groups were used. The catalyst, while soluble in the reaction medium, was also found recyclable, which is an important green feature and a significant step forward from traditional methods that use aluminum chloride.

Bi(OTf)3 was described as an efficient catalyst for the microwave-assisted solvent-free Friedel-Crafts acylation of benzene derivatives with benzoic anhydride [139]. The benzoylation readily occurred with a wide variety of aromatics in short reaction times (Scheme 50). The catalyst was found recyclable and only a negligible activity loss was observed after five consecutive reactions. It was noted that although conventional heating also produced the products it required significantly longer reaction times.

Alkylation: An efficient triflic acid catalyzed one-pot synthesis of N-substituted pyrroles, indoles, and carbazoles was achieved using a successive cyclization/annelation approach [140]. The reaction was carried out applying aryl sulfonamides and 2,5-dimethoxy-tetrahydrofuran as a starting materials (Scheme 51). Although the first step to form pyrroles is a simple cyclization, the subsequent steps to form indoles and carbazoles occurred via the aromatic alkylation and aromatization. The reactant/triflic acid ratio

OMe

O

O O

O

OMe

CH3CN, MW, 45 min

Sc(OTf)3 (10 mol%)dendritic terpyridine ligand

80-99%

R

R

Scheme 49.

MW, 100-160 ˚C, 10-30 min

Bi(OTf)3 (10mol%)

Ph O

O

Ph

O

R RPh

O

62-95%

Scheme 50.

ArS

NH2

O

O O OMeMeO

0.05 eqv. TfOH

1 eqv.TfOH

3.5 eqv.TfOH

CH2Cl2 / RT

SO2Ar

N

SO2Ar

N

SO2Ar

N

80 - 92%

75 - 91%

75 - 86%

Scheme 51.


successfully controlled the formation of the desired product, thus indoles or carbazoles could be prepared without isolating any intermediate product. Despite the use of dichloromethane the rest of the system appears to be green involving a recyclable acid, the one pot-five step reaction (for carbazoles) and the room temperature reactions.

Triflic acid was also found to be an effective catalyst for the preparation of unnatural organofluorine amino acid esters [141]. The highly stereoselective aminoalkylation of indoles and pyrroles was carried out by using chiral 3,3,3-trifluoro-pyruvate-α-methylbenzyl imines. The reaction sequence was completed by a subsequent Pd-catalyzed hydrogenolysis to remove the methyl-benzyl group provided the products in high yields and excellent enantioselectivities. The product α-trifluoromethyl-α-(heteroaryl)-glycine esters were isolated in high yields and excellent enantioselectivity (Scheme 52).

Halogenation: The bromination of aromatic compounds, alkenes and alkynes was achieved using ammonium vanadate as a catalyst using tetrabutylammonium bromide as a bromine source (Scheme 53) [142]. Hydrogen peroxide was applied as an auxiliary oxidant to produce Br2 from the reagent. The process gave a broad variety of products in good yields under mild conditions, e.g. at room temperature. When alkenes and alkynes used the reaction resulted in mixtures. Using alkenes, 1,2-dibromo and hydroxy-bromo products formed, while in the case of alkynes, the reaction stopped at the dibromoalkene phase resulting in the formation of E/Z isomers with high selectivity for the Z-product.

Nitration: Heravi et al. described the nitration of aromatics with vanadium substituted phosphomolibdic acid in acetic anhydride as a solvent using nitric acid as the nitrating agent (Scheme 54) [143]. Although the yields were mostly moderate the catalyst could be reused without significant loss in its activity.

R

+ HNO3Ac2O, reflux

R

NO2

44 -100%

H5[PMo10V2O40]

�Scheme 54.

Bismuth (III) triflate was also found to be an excellent catalyst for the above reaction using toluene as a model substrate [144]. Using dichloroethane as solvent and HNO3 as the nitrating agent the catalyst resulted in complete conversion of the starting material, essentially yielding 100% product. The catalyst was reused in the reaction five times and no activity loss was observed during the subsequent runs. The same reaction could be carried out using N2O5 as a nitrating agent [145].

4.2. Multicomponent Reactions

Reported methods about multi-component sustainable syntheses catalyzed by homogeneous acid catalysts are scarce in the literature. A few acid driven-organic reactions in homogeneous systems are described in this part. Most methods use heteropolyacids, acidic organocatalysts and metal triflates; some other methods use unique homogeneous acid catalysts and constitute isolated examples. It must be noted that although they possess relatively good environ-mental-friendliness, their green potential is not always ideal. The limited number of existing methods, together with the yet-to-be improved sustainability of the presently selected works, illustrates the need for more research in this area.

While ionic liquids are often used as reaction media, their specific properties also allow them to promote different reactions depending on their composition. As a result they have the ability to serve as catalysts as well. For instance, acidic functions can be introduced within the structure of the salt, providing acidic properties. A novel ionic liquid with Brønsted acidic properties was reported by Zare et al. and applied as a catalyst for the three-component synthesis of napthol derivatives [146]. The ionic liquid 1,3-disulfonic acid imidazolium hydrogen sulfate (DsimHSO4) successfully promoted the condensation of β -naphthol with arylaldehydes and alkyl carbamates or amides with high yields in short reaction times (Scheme 55). Despite the controversial eco-friendliness of ILs due mainly to their long and potentially wasteful synthesis, in this study, the IL was used in catalytic amount and was recyclable; consequently it limits the amount of waste generated. In addition, the proposed method has a significantly lower environ-mental impact than other methods often suffering from toxic catalysts in high loading, harsh conditions or long reaction times.

N

F3C

COOEt

NH2

F3C COOEt

N

N

R1

*

R2

R1N

F3C

COOEt

NH2

R2

R1

or

73 - 90%ee 80 - 98%

R2

BzMe

+

2) Pd(OH)2 / EtOH

H2 (5 bar) / 12 h rt

1) TfOH / CH2Cl2 / 2 h - 40 Co

Scheme 52.

R1

H2O2, rt

R

Br

80 -99%

+ Br4N BrNH4VO3

or

R2

orR4

R3

R5

1,2-dibromo and hydroxy-bromo products

Br

Br

or

or

100%

Scheme 53.


Biologically active tetrahydropyridine derivatives were synthesized in presence of a similar ionic liquid ([Py-SO3H]HSO4 - sulfonic acid pyridinium hydrogen sulfate) serving as an eco-friendly catalyst (Scheme 56) [147]. The one-pot three-component condensation of various aromatic aldehydes, aromatic amines and ethyl acetoacetate was carried out without solvent at 100°C to reach yields above 80%. The IL played the role of both Brønsted and Lewis acid to assist the formation of the multiple intermediates. Not only did the reaction proceed better without solvent but the method also proved to be significantly more efficient that previously reported systems using organic solvents and/or toxic catalysts. After extracting the reaction mixture, the IL was used for five consecutive cycles with no noticeable loss of activity.

Polymers are tunable structures that can easily be functionalized. Attaching acidic functions to a polymeric chain forms an interesting material that can potentially be used as a catalyst. A simple and green protocol was reported for the three-

component synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones (Scheme 57) employing the water-soluble and reusable polyvinylsulfonic acid as a Brønsted acid catalyst [148]. This soluble solid-state analogue of sulfuric acid offers many advantages: it has a higher acid density than sulfuric acid, it can be used in aqueous media and has the potential to be recycled, it is cost-effective and easy to handle. As a result, the acid-catalyzed cyclocondensation of aldehydes, ethyl acetoacetate and urea or thiourea was conducted in water at 90°C affording excellent yields. The products were extracted from the mixture and the catalyst could be recycled after simple evaporation of water. The results obtained were comparable and even superior to most conventional metal-based procedures both in terms of yield and reaction rate.

Indium triflate is another metal-triflate with catalytic activity [149]. The four component reaction of aldehydes, isocyanides, azidotrimethylsilane, and aliphatic alcohols was reported using indium triflate as a mild Lewis-acid catalyst (Scheme 58). The

OH Ar H

O

OH

OH

NHAr

NHAr

O R2

O OR1

R1O NH2

O

R2 NH2

O

[Dsim]HSO4 (5 mol%)

solvent free, 80 °C, 7-35 min

91-98%

Scheme 55.

NH2 CHO

OEt

O O

R2R1

2 2

NH

N

OEt

O

R2

R1

R2

R1

[Py-SO3H][HSO4] 15 mol%

solvent free, 100 °C, 30-40 min

87-92%

Scheme 56.

H3C OC2H5

O O

H2N NH2

X

X=O or S

CHO

NH

NHC2H5O

O

X

PVSA

H2O, 90 °C, 60-120 min

CH2-CH

O2S OH

n

85-94%

R

R

Scheme 57.


reaction starts with the Lewis-acid driven formation of carbo-xonium ion intermediate from the aldehyde and the aliphatic alcohol that also serves as a solvent. Interestingly, an optimum catalyst loading was reported for this reaction with yields ranging from moderate to good depending in part on the nucleophilicity of the isocyanide. The reaction shows some green features; it required low catalyst loading of a stable Lewis acid. However, the catalyst was not recyclable and afforded only moderate yields for some substrates. As another drawback of the method; excess amount of some of the reactants was necessary to observe conversion.

A few organocatalyst-driven multi component syntheses were reported under mild conditions in aqueous medium making them interesting methods from the green chemistry perspective. For instance, L-proline is a well-known organocatalyst that has successfully catalyzed multiple organic transformations. Myrboth et al. described the asymmetric multi-component synthesis of chromeno[2,3-d]pyrimidine-triones and xanthene dione derivatives using L-proline as a catalyst [150]. Aromatic aldehydes, dimethyl-cyclohexane-1,3-dione/cyclohexane-1,3-dione and barbituric acid were reacted at room temperature in water to afford chromeno[2,3-d]pyrimidine-triones in good to excellent yields and moderate to high enantioselectivities (Scheme 59). The method was equally successful when using two equivalents of cyclohexane-1,3-dione in place of barbituric acid to form xanthene dione derivatives. The

reaction was mostly assisted by the nucleophilic properties of the amino group of L-proline although its acidic properties contributed. The yields seemed not to be affected by the presence of electron withdrawing or donating substituents. The very mild reaction conditions and the non-toxic nature of the catalyst certainly contribute to reduce the environmental impact of the method despite the relatively high catalyst loading (15%).

The functionalization of organocatalysts with Brønsted acid groups creates acidic organocatalysts suitable to perform con-ventional Brønsted acid-catalyzed reactions. A guanidinium-based sulfonic acid functionalized organocatalyst was developed and proved its effectiveness to replace the traditional liquid mineral acids for the multi-component synthesis of a variety of quinoxaline-, pyrazine- and urazole-derivatives in aqueous media (Scheme 60) [151]. The reactions proceeded smoothly in less than two hours at room temperature or reflux depending on the substrate type. The method also presented the benefits of heterogeneous systems because the product precipitated and was filtered out while the catalyst was extracted from water with ethyl acetate and reused for other cycles with consistent activity.

A similar method was developed by Wang et al. for the synthesis of the polycyclic benzoazulen-1-ones [152]. Although the authors called this procedure “catalyst-free” one should not

R1 CHO R2 NC Me3SiN3

N N

NN

R2

R1

O

R3In(OTf)3 (2 mol%)HC(OMe)3 (1 eq.)

R3OH, 80 °C, 2-6 h(2 eq.) (4 eq.)

45-74%

Scheme 58.

R1

O

O

OR2

R2

NH

NH

O

OO

O

O

O NH

NH

O

O R1 O

O

O OR1

R2

R2

L-proline

Water, RT, 4 h

70-96%

75-85%

Scheme 59.

R1 R2

O R4

R5

NH2

NH2

R3 N CR4

R5 N

HN R1

R2

NH

R3

cat. (5 mol%)

H2O, RT, 50-90 min

73-91%

Scheme 60.


overlook the fact that the solvent acetic acid indeed acted as a mild strength acid catalyst. The microwave activation and the small amount of mild acid represented sufficient conditions to achieve high yields in short times. The substrate scope of the reaction was broad, showing little substituent effect (Scheme 61).

A solvent free A3-coupling was developed for the synthesis of quinolines (Scheme 62) [153]. Microwave heating was used to activate the system and FeCl3 was used as a catalyst. The reaction provided high yields for most substrates, although starting materials with strong electron-withdrawing substituents lowered activity and decreased yields. The environmentally benign catalyst, the high reaction rates and relatively short times are the main green advantages of the process.

Imidazo[1,2-a]pyridines were synthesized by the multi-component Groebke-Bienaymé-Blackburn reaction of 2-amino-pyridines, aromatic aldehydes and isonitriles [154]. With the application of microwave activation, solvent-free conditions and Yb(OTf)3 catalyst the products were obtained in excellent yields in short, only 5 min long, reactions (Scheme 63). The sustainable conditions, the nearly quantitative yield ensured that the environmental impact of this method was significantly lower than that of available alternatives.

A heteropolyacid-catalyzed multicomponent condensation of an aryl aldehyde, acetyl chloride, acetonitrile, and enolizable ketone

for the preparation of β -acetamido ketones (Scheme 64) was described by Tayabee and Tizabi [155]. Several heteropolyacids were screened to compare their relative activity. The vanadium-substituted Keggin-type H5PW10V2O40 achieved the highest yields. Interestingly, despite its lower Brønsted acidity it showed better performance than the traditional Keggin-type heteropolyacid H3PW12O40. In fact, the high catalytic activity is believed to be not only due to the acidity but also to the electron acceptor property of vanadium. Although, the high yields and short reaction times suggest an environmentally friendly protocol, there are a few disadvantages. The reflux conditions, the use of acetonitrile as solvent, as well as the required preparation of the metal-substituted heteropolyacid all increase the overall environmental impact of the protocol.

The heteropoly acid-catalyzed microwave assisted three component aza Diels-Alder cyclization of cyclohexenone, substi-tuted anilines and benzaldehydes to prepare azabicyclo[2.2.2]octan-5-ones (Scheme 65) was described by Borkin et al. [156]. The multistep reaction occurred in a one pot fashion. In the first step a Schiff base formed in situ, which underwent an intermolecular cyclization with the cyclohexenone. Despite the short reaction times the yields were moderate to good and the products formed with excellent diastereoselectivity. The compounds were also tested in preliminary cholinesterase and amyloid β fibrillogenesis inhibition assays to probe them as potential anti Alzheimer’s disease agents.

H2N

H2N

R2

R3

O

O

O

R1O

HOAc (0.1 eq)

Water, MW, 110°C, 7-24 min

HN

NH

O

OR3

R2

R1

70-89%

Scheme 61.

NH2

R1

+O

R2

R3

N

R1

R3

R2

FeCl3 (1mol%)

MW, 120 °C, 40 min

55-95%

Scheme 62.

N NH3

R1R2OHC

R3CNN

N

R1

HN R3

R2

MW, 160 ˚C, 5 min

Yb(OTf)3 (2.5mol%)

95-99%

Scheme 63.

NH

O

O

O O

Cl

O

R

H5PW10V2O40 (0.5mol%)

CH3CN, 80 °C, 0.5-4 h

69-97%

Scheme 64.


4.3. Ring Transformations

The formation of substituted quinolines was described using zinc chloride as the Lewis acid catalyst for the cyclization of ketones with imines (Scheme 66) [157]. The reaction can also be performed as one-pot sequence without prior formation of the starting imines. The quinolines were obtained in moderate yields. Acetic acid was used as the solvent for the reaction allowing the formation of quinolines under environmentally friendly conditions.

Zhao et al. described a green way for the synthesis of substituted 3,2’-tetrahydrofuryl spiroxoindoles through cyclization of 3-allyl-3-hydroxy-2-oxoindoles (Scheme 67) using methanesul-fonic acid (MSA) as catalyst [158]. The reaction did not require any metal and water was used as the solvent. The authors showed that performing the reaction on a gram-scale was easily possible.

The group of Gooßen found that silver triflate was an effective Lewis-acid catalyst for the synthesis of γ-lactones from unsaturated fatty acids (Scheme 68) [159]. The silver served as the catalyst for the migration of the double bond into proper position, as well as a catalyst for the lactone formation. Even though chlorobenzene was used as the solvent, the advantage of the reaction is in the remarkably high yield compared to previous known examples and given that several double bond migration steps have to be achieved before the cyclization can occur. Oligomerization was found to be the major side reaction, however, the formation of δ-lactones was not observed.

OH

O

PhCl, 130°C

AgOTf (15 mol%)

m n O

O

m+n51-72%

Scheme 68.

The synthesis of benzobis-azoles from an aromatic orthoester and diamino diols or dithiols using a Lewis acid catalyst (Scheme 69) was described by Jeffries-EL et al. [160]. Y(OTf)3 was used as environmentally benign catalyst and the desired products where obtained in high yields. The benzobisazoles formed served as monomers for the generation of conjugated polymers for use in organic LED. The drawback from the environmental point is that a pyridine/THF mixture had to be used as solvent for the reaction.

Uozumi and co-workers showed that camphorsulfonic acid (CSA) can be used as efficient catalyst for the synthesis of 4(3H)-quinazolinones [161]. The reaction used a water-ethyl lactate mixture as green solvent and was able to produce the desired compounds from a large variety of 2-aminobenzamides and 1,3-diketones (Scheme 70). The diketones used can be both cyclic and acyclic and they undergo a C-C bond cleavage during the reaction.

The solvent- and metal-free synthesis of quinolines using a Brønsted acid was demonstrated by Bao et al. [162]. N-alkylamines were reacted with alkenes or alkynes and a catalytic amount of triflic acid to afford the formation of the quinolines in high yields (Scheme 71). The reaction did not require any solvent and used oxygen as a green oxidant.

The group of Jirgenson developed a Lewis acid-catalyzed protocol for the formation of vinyloxazolines and vinyloxazines [163, 164]. Using bis(imidates) as starting materials the formation of the desired products was possible using a catalytic amount of FeCl3 or AlCl3

(Scheme 72). The products were obtained in high yields and short reaction times. While the use of iron chloride is still acceptable within green chemistry, the use of aluminium chloride and dichloromethane should be avoided. The same group could also show that bis(trichloroacetimidate) can serve as starting material for the reaction [165].

O

+ +

10% H4[SiW12O40]

MW, CH3CNN

O

R

10 min, 100°C

NH2

R1 R2

R2

R1

49 - 75%endo/exo up to 96:4

Scheme 65.

52-64%

AcOH, reflux N

NX Y

O

X

Y

ZnCl2

R

R

Scheme 66.

70-92%

H2O, reflux

MSA (20 mol%)

N

HO

R3

R4

R2

O

N

R2

O

O

R4 R3

R1R1

Scheme 67.


Cossy et al. demonstrated that iron and indium salts can serve as effective Lewis acid catalysts for the cyclization of tert-butyl carbonates to form cyclic carbonates [166]. Both five- and six-membered cyclic carbonates can be formed using this method. While iron proved to be effective for substrates containing only carbon and hydrogen, indium was shown to be superior when heteroatoms are present in the starting material (Scheme 73). The syn diastereomer was always the major product obtained, albeit the selectivity was moderate in certain cases. Another drawback of the method was the use of the not-green solvent acetonitrile.

A scandium triflate catalyzed [3+3] annulation to form tetrahydro-β-carbolines and tetrahydroisoquinolines was developed by Wang et al. [167]. The transformation used benzylic alcohols and aziridines as substrates to give the desired products in moderate yields (Scheme 74). The [3+3] process applied allows for greater product diversity than previously established methods. While scandium triflate can be considered a green Lewis acid, the use of 1,2-dichloroethane as solvent counterbalances the overall environmental friendliness of the procedure.

pyridine, THF, 60 ˚C

Y(OTf)3 (5 mol%)

78-84%

S

C(OEt)3

Br

C8H17

ClH3N NH3Cl

OHHO

XH NH3Cl

XHClH3N

or

N

X N

X

S

S Br

C8H17Br

C8H17

N

O O

N

S

S Br

C8H17Br

C8H17

or

Scheme 69.

H2O - ethyl lactate, 100 ˚C

CSA (10 mol%)

NH2

NHR2

R1

O

N

N

R1

O

O O

R3

R2

O

R3

Scheme 70.

HN

R1

R2 N R2

R3

R3 TfOH (15 mol%)

no solvent, O2, 120 ˚C

R1

61-98%

or

R3

Scheme 71.

AlCl3 or FeCl3 (10 mol%)

CH2Cl2, RT

68-98%

O

Cl3C

NH

O

CCl3

HN

R1n

NO

R1

CCl3

nR2

R2

Scheme 72.

R1

OBoc

R2

OAc

n

O O

O

R1

nR2

FeCl3 or InCl3 (10 mol%)

CH3CN, RT

37-98%, 60:40-75:25 syn:anti

Scheme 73.


A new strategy for the en-yne-cyclizations was developed by Zhang and co-workers [168]. Instead of the traditional π-activation they chose to use a Brønsted acid to perform σ-activation of alkyne enones to trigger the cyclization and yield the desired 5-membered ring products (Scheme 75). Depending on the starting material used, both saturated and unsaturated ring systems were obtained in moderate to high yields. While the initial cyclization yielded a mixture of syn and anti-isomers; a base-catalyzed isomerization led to the selective formation of the anti-isomer. Depending on the substrate, 1,2-dichloroethane or nitromethane had to be used as the solvent which increased the environmental impact of the reaction.

Lithium bromide was applied as Lewis acid catalyst for the ring expansion of epoxides with α-mercaptocarboxylic acids to form 1,4-oxathian-2-ones (Scheme 76) [169]. The reaction proceeded under solvent-free conditions at room temperature resulting in the products in high yields. The epoxide opening was achieved with high regioselectivity and the catalyst was recovered after the reaction and reused without any loss of efficiency.

The ring-opening reaction of epoxides with ammonium thiocyanate was efficiently catalyzed by a PEG-supported sulfonic acid [170]. The water soluble polymer combines the best features of homogeneous catalysis with the easy separation of a heterogeneous catalyst. The reaction was carried out under mild conditions in water as the solvent and formed the β-hydroxy thiocyanates in excellent yields (Scheme 77). High regioselectivities were obtained during the opening of the epoxide.

O

R water, RT

PEG-SO3H (10 mol%)

84-96%

NH4SCNHO

R SCN

�Scheme 77.

Nazari et al. described that a similar reaction of epoxides can also be catalyzed by imidazole-1-yl-acetic acid [171]. Ammonium thiocyanate and sodium azide was used as reagents for the ring opening reaction (Scheme 78). The catalyst used was recycled after the reaction and reused for consecutive reactions without significant loss of activity. The products were obtained with high regioselectivity in most cases.

O

R water, reflux

(30 mol%)

82-88%

NH4SCN

HO

R N3

orNaN3

N

N OH

O

HO

R SCNor

�Scheme 78.

N

NTsAr

OH

R2

R3

OH

R1 R2

Sc(OTf)3 (5 mol%)

1,2-DCE, reflux1,2-DCE, reflux

Sc(OTf)3 (2 mol%)

R3

R2

NTs

Ar

38-76%

N

R2R1

NTs

Ar

46-77%

Scheme 74.

XR2

OR1

X

R1

O R2

O

1) TfOH (2.5 mol%), DCE (wet), RT - 70 ˚C

2) DBU, DCE, RT

51-84%

R2

OR1R1

O R2

OTfOH (2.5 mol%)

81-99%

OPivCH3NO2, RTn

n

Scheme 75.

O

R1

OHO

R2HS S

O

R1

O

R2no solvent, RT

LiBr (10 mol%)

77-93%

Scheme 76.


The ring opening of epoxides with aromatic amines (Scheme 79) was described by Halimehjani et al. using boric acid and glycerol as a green catalytic system in water as the solvent [172]. The reactions proceeded with high yields and high regioselectivities under mild conditions. Glycerol acts as chelating agent for the boric acid thus increasing its acidity.

The catalytic etherification of glycidol with different alcohols (Scheme 80) was described by Capacchione et al. [173]. Using a very low loading of Al(OTf)3 as the catalyst the monoalkyl glycerol ethers were obtained in mostly high yields. The etherification happens preferentially at the terminal position, although the ratio between terminal and internal alkylation was not very high in many cases. The alcohol used for alkylation additionally served as the solvent, no other solvent was needed for the reaction.

Majee and co-workers developed a method for the ring-opening of aziridines with various nucleophiles (Scheme 81) using an imidazole-based zwitterionic organocatalyst [174]. The catalyst acts as hydrogen donor to activate the aziridine towards the attack of the nucleophile. No solvent was needed for the reaction of carbon-, oxygen- and nitrogen-nucleophiles and the products were obtained in high yields and high regioselectivities with concern to the position of ring opening.

Iron chloride was used as the Lewis acid catalyst in the ring-opening polymerization of cyclic lactones by Chakraborty and Gowda [175]. The authors showed that ε-caprolactone, δ-

valerolactone and β-butyrolactone can be polymerized effectively (Scheme 82) to form polymers with a narrow molecular weight distribution. Through the addition of alcohols and the variation of the monomer-catalyst ratio the polymer properties can easily be tuned.

O

O

nRO

OR

O

nRT

FeCl3ROH

�

Scheme 82.

The ring-opening alternating co-polymerization of cyclic anhydrides and epoxides (Scheme 83) was described using a Lewis acid-base pair as catalytic system under solvent-free conditions [176]. The combination of an organozinc compound with a N-heterocyclic organobase catalyzed the polymerization in most cases with high conversions, extremely high degree of alternation and a narrow molecular weight distribution.

The transformation of furfuryl alcohol to alkyl levulinates also readily occurred in methanol with microwave activation [177]. Several metal salts, including CrCl3, ZnSO4, AlCl3, or Al2(SO4)3 were tested as catalysts. Al2(SO4)3 showed the best performance, likely due to its somewhat elevated Brønsted acidity. The high dielectric constant of the solvent, probably contributed to the

O

R1 water, 35°C

B(OH)3 (30 mol%)glycerol

73-100%

NH2

R2

HN

R2

R1

OHHN

R2

OH

R1

or

Scheme 79.

O OHR

OH Al(OTf)3 (0.01 mol%)

no solvent, 80°C

O OHR

OH

HO OH

OR

67-98% (2:1 - 7:2)

Scheme 80.

TsN

R1 no solvent, 60-85°C

76-84%

N

R2R3

or

R5

HN

R6

R4OH

or

N

R2R3

R1

NHTs

R4O

R1

NHTs

78-82%

R1

NHTs

R5N

R6

75-85%

N N SO3(10 mol%)

Scheme 81.


efficiency of the alcoholysis of furfuryl alcohol via its strong microwave absorption ability that ensured that in a 5 min reaction at 150°C, the reaction occurred (Scheme 84) in 80% yield and nearly exclusive selectivity. During mechanistic investigations of the reaction mechanism key intermediates (methoxymethylfuran (MMF) and 4,5,5-trimethoxypentan-2-one (TMP)) were isolated. The catalyst was reused for six consecutive cycles with negligible loss in activity. Thus despite using DCM as solvent in the work up the method is rapid, efficient and partially environmentally benign.

O OH Al2(SO4)3

MeOH, MW, 150°C, 5min

OMe

O

O

80%

Scheme 84.

4.4. Asymmetric Synthetic Applications

Catalysis by chiral phosphoric acids: Huang et al. showed that the catalytic asymmetric synthesis of chiral 1,3-butadienyl-2-carbinols was possible by using a chiral phosphoric acid as a catalyst [178]. The reaction between aldehydes and homoallenyl-boronates (Scheme 85) did not require the use of a metal catalyst and furnished the products in excellent yields and enantio-selectivities. The reaction was performed on a gram scale and the products were of interest due to their synthetic utility as shown by the authors through the synthesis of a NCSi-gb analogue using their methodology.

The generation of chiral quaternary centers was achieved by List et al. Chiral phosphoric acids enantioselectively catalyzed the α-amination of α-branched ketones (Scheme 86), a transformation that cannot easily be achieved by traditional amine-catalysis [179]. High yields and good enantioselectivities were obtained for the amination in the α-position of several different cyclic α-branched ketones with diazocarboxylates.

A solvent free variation of the above reaction was published by Toste et al. using a different chiral phosphoric acid [180]. Proper mixing was achieved by dissolving the starting materials in CH2Cl2. After evaporating the solvent, the residue was heated at 45°C for 40-60 h to obtain the α-aminated products in high yield and high enantioselectivities.

Chiral phosphoric acids were also applied for the Friedel-Crafts addition of benzoxazinones with substituted pyrroles (Scheme 87) [181]. The products were formed in high yields and enantio-selectivities generating a quaternary stereocenter. The presence of the CF3-group seems to be essential as it contributes to hydrogen binding in the activation mode of the reaction.

The asymmetric Friedel-Crafts addition of acetals to naphthols (Scheme 88) was described by Da et al. [182]. Using a chiral phosphoric acid as catalyst and acetic acid as a co-catalyst the addition products were obtained in moderate yields and enantioselectivities. Even though the reaction was performed in dichloroethane as a solvent, the major benefit of the applied system was that the reaction could be performed under mild conditions.

OO

R1 R1

OO

R2 R3O

O

O

R1

R1

O R2

R3

no solvent, 110 ˚Cn

Zn(C6F5)2 / DMAP

Scheme 83.

(5 mol%)

92-99%, 90-99%ee

toluene, 4A MS, -60 ˚C

2,4,6-iPrC6H2

2,4,6-iPrC6H2

O

OP

O

OH

O

B

OR

OH

R H

O

Scheme 85.

Ar

OO

PO

OH

Ar

Ar = 9-phenanthryl

(5mol%)

CH3CN, RT

N

NCO2R2

R2O2CO

R1

n

n = 1-4

O

R1

nN NHCO2R2

CO2R2

40-99%, 20-98%ee

Scheme 86.


The asymmetric transfer hydrogenation of a range of imines could also be catalyzed by chiral phosphoric acids. The enantioselective hydrogenation of different substituted quinolines (Scheme 89) was shown by Rueping and his coworkers using only 0.5mol% of a chiral phosphoric acid as a catalyst [183]. Both a traditional batch reactor and a continuous-flow system were able to perform the reaction with the latter significantly improving the reaction yield (67 vs. 97%). More and Bhanage showed that the sustainable solvent diethyl carbonate could be used for the same reaction [184]. Similar high yields and enantiomeric excesses were obtained using a Hantzsch ester as the hydrogen donor.

A binaphthol-derived phosphoric acid in combination with a cinchona alkaloid derived amine was an effective catalytic system for the enantioselective epoxidation of α,β-unsaturated aldehydes (Scheme 90) yielding the products in moderate to high yield and high enantioselectivities [185]. Although the reaction was per-formed in THF, a not-green solvent, the system benefits from the use of hydrogen peroxide as an oxidant and the fact that the aldehyde could be used as a substrate, which is often not possible using other protocols due to the oxidation of the carbonyl group.

The enantioselective epoxidation of enynes was performed by using scandium triflate as the Lewis acid in presence of a chiral N,N’-dioxide as ligand [186]. The selective epoxidation of the

alkene (Scheme 91) was achieved in excellent yields and enantioselectivities using hydrogen peroxide as the oxidant. A low catalyst loading of 0.5% was applied and the reaction could also easily be performed on a gram scale. The high selectivity towards the alkene epoxidation overcomes the drawbacks associated with the synthesis of the ligand and the use of THF as a solvent.

Using ZnCl2 as a Lewis acid in combination with a prolineamide as chiral catalyst the asymmetric aldol reactions of aromatic aldehydes with ketones (Scheme 92) was described in high yields, syn:anti ratios and enantiomeric excess [187]. In addition to the use of an environmentally benign catalyst the system also benefited from the use of a 1:1 water-ethanol mixture as a solvent system.

Penhoat et al. showed that this reaction can also be performed using unmodified proline and ZnCl2 as Lewis acid [188]. The study had a smaller substrate scope and DMSO had to be used as a co-solvent making this approach less appealing from a sustainability point of view than the before mentioned ZnCl2-prolineamide system.

An environmentally friendly variation of the Mukaiyama aldol reaction was developed by Kobayashi and his co-workers [189]. It was shown that a large variety of Lewis acids can be used for the reaction of aldehydes with silyl enol ethers (Scheme 93) in combi-

O

N

O

R1

NH

R2

CF3

O

HN

O

R1

CF3

NH

R2

toluene, RT

(5mol%)

OO

PO

OH

2,4,6-(iPr)3C6H2

2,4,6-(iPr)3C6H2

85-96%, 87-97%ee

Scheme 87.

(20 mol%)AcOH (20 mol%)

42-72%, 20-71%ee

C2H4Cl2, 35 ˚C

2,4,6-iPrC6H2

2,4,6-iPrC6H2

OO

PO

OH

OH2

R2

OMe

OMeR1

OH

R1

*MeO R2

Scheme 88.

N R2

R1

NH

CO2EtEtO2C

NH

R2

R1

Ar

OO

PO

OH

Ar

Conditions: Yield:Catalyst (0.5 mol%): Ar = 9-phenantryl 91-97%, 94-99%eeCHCl3, 60 °C, microreactor

Catalyst (2 mol%): Ar = 2,4,6-iPr3C6H2 91-99%, 87-99%eediethylcarbonate, -10 °C

Conditions

Scheme 89.


50% aq. H2O2 (5 equiv.)THF, 50 °C

O

O

POH

O

R

R

N

NH2

N

MeO

R = Ph or 2,4,6-iPr3Ph (10 mol%)

43-94%, 70-98%ee

H

O

R1

R2

O

R2

R1 H

O

Scheme 90.

(0.5 mol%)Sc(OTf)3 (0.5 mol%)

90-97%, 95-99%ee

H2O2 (30% aq.), THF, 35 °C

R1

O

R2

R3

R1

O

R2

R3

N

NH

O

ON

NH

O

OiPr

iPr Pri

iPr

O

Scheme 91.

R1

(10 mol%)

ZnCl2 (10 mol%)

80-99%, 18:82-1:99 syn:anti85-99%ee

EtOH-H2O (1:1)R2

R3

OO

NNHPh

Ph

O

NH

R2

R3

O OH

R1

TFA

Scheme 92.

R1

(4 mol%)

Fe(OTf)2 (3 mol%)

pyridine (7 mol%)

81-99%, 88:12-98:2 syn:anti80-99%ee

DME-H2O (7:3)R3 H

OOSiMe3

R3

R2

OH O

R1

R2

N N

OH HOBut tBu

Scheme 93.

nation with a chiral bipyridine ligand. The environmentally friendly metal ions iron and bismuth showed especially good results using an aqueous solvent system. The desired aldol products were obtained in high yields and excellent syn:anti selectivities as well as enantiomeric excess.

The asymmetric Michael addition using a catalyst made of Yb(OTf)3 as Lewis acid and L-proline as a chiral ligand (Scheme 94) afforded the corresponding addition products with yields up to 94% and high enantioselectivities under environmentally friendly conditions [190]. The reaction was performed in water as a solvent


and the aqueous phase, containing the catalyst, was recycled several times without appreciable loss of catalytic activity.

An asymmetric version of the Strecker reaction using a chiral Brønsted acid was described by Barbero et al. [191]. The use of substituted o-benzenedisulfonimides as a chiral catalyst allowed the formation of the α-aminonitrile from acetophenones, anilines and TMSCN in high yields and enantiomeric excess (Scheme 95). The reaction was performed under solvent-free conditions and the catalyst was recycled three times without decrease in yield or enantioselectivity.

Using a chiral Mg(OTf)2-BOX complex as a Lewis acid catalyst the formal [3+2] cycloaddition to form chiral γ-lactams (Scheme 96) was possible in mostly high yields and enantio-selectivities [192]. While the use of the imine was necessary for the success of the reaction, both stereoisomers of the imine could be used as starting material in the reaction, a separation was not necessary. A drawback from the green point of view is the need for diethylether as solvent in the reaction.

4.5. Miscellaneous Reactions

The combined application of acidic organocatalysis and heterogeneous catalytic hydrogenations allowed to solve a long standing problem the hydrogenation of indoles under aqueous conditions [193]. The typical conditions for indole hydrogenation are somewhat harsh and often result in indole over-hydrogenation. The reaction was carried out at ambient temperature in water as a solvent by using pTSA as an acidic organocatalyst that protonated indole and made it soluble in the aqueous phase. The protonation also destabilized the aromatic system helping the subsequent hydrogenation step (Scheme 97) to produce the products in high yield.

The N-formylation of amines (Scheme 98) was achieved in a ZnCl2 initiated Lewis acid-catalyzed process [194]. The reactions proceeded without any solvent and the products were obtained in moderate to high yields. Both aromatic and aliphatic amines were successfully used as substrates for the reaction.

L-proline (12 mol%)

Yb(OTf)3 (5 mol%)

H2O, 90 ˚C

29-94%, 17-79%ee

R3

O

R4

O

R1R2

O

R3O

R4

O

R1 R2

O

Scheme 94.

no solvent, -20 ˚C

61-88%, 87-97%ee

O

R2

NH2

TMSCNHN

R2CN

SO2

NH

O2S

(5 mol%)

R1 R3

R1

R3

Scheme 95.

(10 mol%)

Mg(OTf)2 (10 mol%)

4A MS, Et2O, 0˚C

26-98%, 23-99%ee

CO2R1R1O2C

NCO R2 R3

N

MeO

O

N N

O

Ph

Ph

Ph

Ph HN

R2

R3

NH

O

OMe

R1O2C

R1O2C

Scheme 96.

Pt/C, H2, pTSA, H2O

rt, 10-50 bar, 3 h

68 - 96%

NH

R1

R2

NH

R1

R2

NH

R1

R2

H H

A

pTSA

H2

- pTSA

Scheme 97.


NH2

R1

O

HO H no solvent, 70°C

ZnCl2 (10 mol%)

60-98%

NH

R1

H

O

�Scheme 98.

While ZnCl2 was also used as the catalyst for the amide formation between fatty acids and long-chain amines (Scheme 99), Sugi and co-workers showed that FeCl3 performed slightly better in this transformation [195]. Using 20 mol% of the catalyst, the desired amides were obtained in mainly high yields. The use of the not-green solvent mesitylene was needed to remove water during the reaction to ensure complete conversion of the starting materials.

OH

O

H2N

n n

m

m NH

O

mesitylene, reflux

FeCl3 (20 mol%)

47-93% �Scheme 99.

Another amidation reaction, using alcohols and nitriles (Scheme 64) was described in a Ca(II) triflate-catalyzed Ritter reaction (Scheme 100) [196]. The solvent-free microwave-assisted reaction resulted in high yields in short reaction times for a variety of alkyl and aryl substituted alcohols and nitriles. The reaction required the presence of a phase transfer agent (Bu4NPF6) which was thought to be necessary to activate the hydroxyl group.

OHR2

R3

R1

N R4

MW, 120°C, 15 min

Ca(OTf)2 (5mol%)Bu4NPF6 (5mol%)H2O (2 equiv)

NH

R2R3

R1 R4

O

65-96%

Scheme 100.

Gu et al. showed that aqueous solutions of gluconic acid acted as a promoting medium for various reactions [197]. Amongst others, the Michael addition of indoles with various α,β-unsaturated compounds (Scheme 101) was performed under milder conditions than previously reported. The reaction medium not only allowed to obtain the products in moderate to excellent yields, but also eased

the separation of the product to a simple extraction. The reaction medium could then be reused for several runs without decrease in reaction yield.

Simple amine hydrochlorides were demonstrated to be efficient, mild acid catalysts. Pyridium hydrochloride was found to be the catalyst of choice for the syntheses of tungsten tert-butylimido and adamantylimido alkylidene complexes, which are potential alkene methathesis catalysts [198].

The conversion of biomass to produce chemicals is becoming more-and-more attractive due to the need of identifying new non-petroleum based feedstock. While the advantages of using such biodegradable and abundant starting materials are obvious, the methods to transform them often used corrosive mineral acids. Research to develop new protocols offering lower environmental impact is in the forefront of biomass related research.

The cyclization of sorbitol to isosorbide (Scheme 102) was successfully developed in a microwave-assisted transformation in ionic liquids [199]. The best performing IL was N,N,N-trimethyl-N-propylammonium-bis(trifluoromethylsulfonyl)amide ([TMPA][NTf2]). Under optimized conditions the product yield was above 60% when the reaction was performed at 180°C for 10 min with a catalytic amount of p-toluenesulfonic acid. The IL likely improved the nucleophilicity of the substrate. The IL could be recycled for up to five times with only a negligible drop in yields. Although the reaction conditions are mostly green, the recovery process required the use of dichloromethane and thus contributed to the waste generation.

In similar processes the microwave-assisted dehydration of sugars by niobium and zirconium phosphates [200] and mesoporous SBA-15 catalysts [201] resulted in the formation of 5-hydroxy-methyl-furfural.

Based on the above surveyed results, the applications of water stable solid acids, although substantial in the reviewed period, probably are less extensive than those with solid acids. The well-known examples, such as heteropoly acids and metal triflates still dominate this field. Most of the new developments occurred in the area of organocatalysis especially in asymmetric organocatalysis. The introduction of the BINOL-based chiral phosphoric acids significantly extended the application possibilities and aided the expansion of this field that was led by chirally modified Lewis acids for an extended period. The future developments must address, however, the significant challenges these new catalysts face, in order to extend their applications, potentially, to the industrial level.

N

R1 R3

O

R4

H2O, 100°CR2

N

R1R2

R3

O

R4

58-99%

gluconic acid

Scheme 101.

O

O

H

H

OH

HO

HO

OH

OH

OH

OH

OH

p-TsOH (5mol %)

[TMPA][NTf2], MW, 180°C, 10 min

62%

Scheme 102.


CONCLUSIONS

Recent advances in the application of environmentally benign acid catalysts have been reviewed. Due to the importance and magnitude of the contribution of the acid-catalyzed reactions to the development of sustainable synthetic methods, the topic remains at the forefront of synthesis research. The focus of new developments is finding novel applications for traditional reactions that occur under obsolete and unsustainable conditions. While the directions during the nearly 150 years of acid catalysis substantially changed over the past decades, the applications of acid catalysts will remain an important tool in organic synthesis development. Hence, the continuous development of green acid catalytic processes will likely be one of the major driving forces in the growth of sustainable synthesis development for the preparation of pharmaceuticals, fine chemicals and materials.

CONSENT FOR PUBLICATION

Not applicable.

FUNDING

None.

CONFLICT OF INTEREST

The authors confirm that this article content has no conflict of interest.

ACKNOWLEDGEMENTS

Support of our work by the University of Massachusetts Boston is gratefully acknowledged.

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